Amide derivatives, process for preparation thereof and use thereof as insecticide

ABSTRACT

A compound represented by Formula (1): 
     
       
         
         
             
             
         
       
     
     The compound can be used as insecticides.

This application is a DIV of Ser. No. 10/587,990 filed Jun. 6, 2007, now U.S. Pat. No. 8,168,825, which is a 371 of PCT/JP2004/019770 Dec. 24, 2004.

TECHNICAL FIELD

The present invention relates to a compound represented by Formula (1):

wherein A₁, A₂, A₃ and A₄ each represent a carbon atom, a nitrogen atom or an oxidized nitrogen atom;

R₁ and R₂ each represent a hydrogen atom, an optionally substituted alkyl group or an optionally substituted C1-C4 alkylcarbonyl group;

G₁ and G₂ each represent an oxygen atom or a sulfur atom;

X, which may be identical or different, represents a hydrogen atom, a halogen atom, a C1-C3 alkyl group or a trifluoromethyl group;

n is an integer of 0 to 4; and

Q₁ and Q₂ each represent an optionally substituted phenyl group, an optionally substituted naphthyl group or an optionally substituted heterocyclic group,

an insecticide comprising the compound as the active ingredient, and a process for preparation thereof and use thereof.

BACKGROUND ART

International Publication WO 2000/55120 and U.S. Pat. No. 6,548,514 describe a compound similar to the compound of the present invention for the use as medicament, but they do not describe on the insecticidal activity of the compound. The compound clearly does not fall within the scope of claims of the present invention.

International Publication WO 2000/7980 describes a compound similar to the compound of the present invention for the use as medicament, but it does not describe on the insecticidal activity of the compound. The compound clearly does not fall within the scope of claims of the present invention.

US Patent Laid-Open No. 2002-032238 describes a compound similar to the compound of the present invention for the use as medicament, but it does not describe on the insecticidal activity of the compound. The compound clearly does not fall within the scope of claims of the present invention.

DISCLOSURE OF THE INVENTION

The object of the present invention is to provide a pesticide having a high insecticidal efficacy. Another object of the present invention is to provide a compound represented by Formula (1), a process for preparation of the compound, an insecticide comprising the compound as an active ingredient, and a process for controlling pests by using a combination of the compound with another pesticide and/or a fungicide.

The inventors have conducted intensive studies to solve the above problems and discovered that the compound of the invention is a novel compound unknown in the documents and has remarkably excellent insecticidal effects, thus finding a novel application of the compound as a pesticide. Further, they also discovered that a compound unknown in the documents is a useful intermediate for the preparation of the compound of the present invention. As a result, they have completed the present invention.

The subject of the invention is as follows.

[1] A compound represented by Formula (1):

wherein A₁, A₂, A₃ and A₄ each represent a carbon atom, a nitrogen atom or an oxidized nitrogen atom;

R₁ and R₂ each represent a hydrogen atom, an optionally substituted alkyl group or an optionally substituted C1-C4 alkylcarbonyl group;

G₁ and G₂ each represent an oxygen atom or a sulfur atom;

Xs, which may be identical or different each other, represent a hydrogen atom, a halogen atom, a C1-C3 alkyl group or a trifluoromethyl group;

n is an integer of 0 to 4; and

Q₁ represents an optionally substituted phenyl group, an optionally substituted naphthyl group or an optionally substituted heterocyclic group;

Q₂ represents a phenyl group or heterocyclic group having one or more substituents, at least one of the substituent being any of a C1-C4 haloalkoxy group, a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group and a C1-C6 perfluoroalkylsulfonyl group.

[2] The compound as described in [1] represented by Formula (1), wherein

R₁ and R₂ are each a hydrogen atom, a C1-C4 alkyl group or an optionally substituted C1-C4 alkylcarbonyl group;

Xs, which may be identical or different each other, are a hydrogen atom, a halogen atom or a trifluoromethyl group;

Q₁ is a phenyl group, or a substituted phenyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group, and a phenyl group; a heterocyclic group (the heterocyclic group herein represents a pyridyl group, a pyridin-N-oxide group, a pyrimidinyl group, a pyridazyl group, a pyrazyl group, a furyl group, a thienyl group, an oxazolyl group, an isoxazolyl group, an oxadiazolyl group, a thiazolyl group, an isothiazolyl group, an imidazolyl group, a triazolyl group, a pyrrolyl group, a pyrazolyl group or a tetrazolyl group), or a substituted heterocyclic group (which means the same as those described above) having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group, and a phenyl group;

Q₂ is represented by Formula (2):

(wherein Y₁ and Y₅, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₃ represents a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group or a C1-C6 perfluoroalkylsulfonyl group; and Y₂ and Y₄ each represent a hydrogen atom, a halogen atom or a C1-C4 alkyl group);

or by Formula (3):

(wherein Y₆ and Y₉, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₈ represents a C1-C4 haloalkoxy group, a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group or a C1-C6 perfluoroalkylsulfonyl group; and Y₇ represents a hydrogen atom, a halogen atom or a C1-C4 alkyl group).

[3] The compound as described in [2], represented by Formula (1a), which is Formula (1) with A₁, A₂, A₃ and A₄ being all carbon atoms:

wherein R₁, R₂, G₁, G₂ and Q₁ have the same meanings as those described in [2], and Q₂ is represented either by Formula (2):

(wherein Y₁ and Y₅, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₃ represents a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group or a C1-C6 perfluoroalkylsulfonyl group; and Y₂ and Y₄ each represent a hydrogen atom, a halogen atom or a C1-C4 alkyl group);

or by Formula (3):

(wherein Y₆ and Y₉, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₈ represents a C1-C4 haloalkoxy group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group or a C1-C6 perfluoroalkylsulfonyl group; and Y₇ represents a hydrogen atom, a halogen atom or a C1-C4 alkyl group),

wherein in Formula (1a), X₁ and X₂ each represent a hydrogen atom or a fluorine atom; and

X₃ and X₄ represent a hydrogen atom.

[4] The compound as described in [3], represented by Formula (1a), wherein

Q₁ is a phenyl group; a substituted phenyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group; a pyridyl group; or a substituted pyridyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group.

[5] The compound as described in [1] or [2], represented by Formula (1a), which is Formula (1) with A₁, A₂, A₃ and A₄ being all carbon atoms:

wherein Q₂ is represented either by Formula (2):

(wherein Y₁ and Y₅, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₃ represents a C2-C6 perfluoroalkyl group; and Y₂ and Y₄ each represent a hydrogen atom, a halogen atom or a C1-C4 alkyl group);

or by Formula (3):

(wherein Y₆ and Y₉, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₈ represents a C2-C6 perfluoroalkyl group; and Y₇ represents a hydrogen atom, a halogen atom or a C1-C4 alkyl group);

X₁ and X₂ each represent a hydrogen atom or a fluorine atom;

X₃ and X₄ represent a hydrogen atom;

one of R₁ and R₂ is a hydrogen atom, the other is a C1-C4 alkyl group or an optionally substituted C1-C4 alkylcarbonyl group, or both of them are independently a C1-C4 alkyl group or an optionally substituted C1-C4 alkylcarbonyl group;

G₁ and G₂ each represent an oxygen atom or a sulfur atom; and

Q₁ represents a phenyl group; a substituted phenyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group; a heterocyclic group (the heterocyclic group herein represents a pyridyl group, a pyridin-N-oxide group, a pyrimidinyl group, a pyridazyl group, a pyrazyl group, a furyl group, a thienyl group, an oxazolyl group, an isoxazolyl group, an oxadiazolyl group, a thiazolyl group, an isothiazolyl group, an imidazolyl group, a triazolyl group, a pyrrolyl group, a pyrazolyl group or a tetrazolyl group); or a substituted heterocyclic group (which means the same as those described above) having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group.

[6] The compound as described in [5], represented by Formula (1a), wherein

Q₁ is a phenyl group; a substituted phenyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group; a pyridyl group; or a substituted pyridyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group.

[7] The compound as described in [1] or [2], wherein A₁ is a nitrogen atom or an oxidized nitrogen atom; A₂, A₃ and A₄ are a carbon atom; R₁ and R₂ are each a hydrogen or a C1-C4 alkyl group; X is a hydrogen atom and a fluorine atom; n is 0 or 1; and G₁ and G₂ are an oxygen atom.

[8] The compound as described in [7], represented by Formula (1), wherein

Q₁ is a phenyl group; a substituted phenyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group; a pyridyl group; or a substituted pyridyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group.

[9] A compound represented by Formula (4):

wherein A₁, A₂, A₃ and A₄ each represent a carbon atom, a nitrogen atom or an oxidized nitrogen atom;

R₁ represents a hydrogen atom, a C1-C4 alkyl group or a C1-C4 alkylcarbonyl group;

G₁ and G₂ each represent an oxygen atom or a sulfur atom;

X, which may be identical or different each other, represents a hydrogen atom, a halogen atom, an optionally substituted C1-C3 alkyl group or a trifluoromethyl group;

n represents an integer of 0 to 4;

Q₁ represents a phenyl group; a substituted phenyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group; a heterocyclic group (the heterocyclic group herein represents a pyridyl group, a pyridin-N-oxide group, a pyrimidinyl group, a pyridazyl group, a pyrazyl group, a furyl group, a thienyl group, an oxazolyl group, an isoxazolyl group, an oxadiazolyl group, a thiazolyl group, an isothiazolyl group, an imidazolyl group, a triazolyl group, a pyrrolyl group, a pyrazolyl group or a tetrazolyl group); or a substituted heterocyclic group (which means the same as those described above) having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group or a phenyl group; and

Hal represents a chlorine atom or a bromine atom.

[10] A process for preparation of the compound represented by Formula (1) as described in [1], wherein the compound represented by Formula (4) as described in [9] is reacted with a compound represented by Formula (5):

(wherein R₂ represents a hydrogen atom, an optionally substituted alkyl group or an optionally substituted C1-C4 alkylcarbonyl group; and

Q₂ represents an optionally substituted phenyl group, an optionally substituted naphthyl group or an optionally substituted heterocyclic group).

[11] A compound represented by Formula (6):

wherein A₁, A₂, A₃ and A₄ each represented by a carbon atom, a nitrogen atom or an oxidized nitrogen atom;

R₁ and R₂ each represent a hydrogen atom, a C1-C4 alkyl group or a C1-C4 alkylcarbonyl group;

G₂ represents an oxygen atom or a sulfur atom;

X, which may be identical or different, represents a hydrogen atom, a halogen atom, an optionally substituted C1-C3 alkyl group or a trifluoromethyl group;

n represents an integer of 0 to 4;

Q₂ is represented either by Formula (2):

(wherein Y₁ and Y₅, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₃ represents a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group or a C1-C6 perfluoroalkylsulfonyl group; and Y₂ and Y₄ each represent a hydrogen atom, a halogen atom or a C1-C4 alkyl group);

or by Formula (3):

(wherein Y₆ and Y₉, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₈ represents a C1-C4 haloalkoxy group, a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group or a C1-C6 perfluoroalkylsulfonyl group; and Y₇ represents a hydrogen atom, a halogen atom or a C1-C4 alkyl group).

[12] A process for preparation of the compound represented by Formula (1) as described in [1], wherein the compound represented by Formula (6) as described in [11] is reacted with a compound represented by Formula (7):

(wherein G₁ represents an oxygen atom or a sulfur atom; Q₁ represents a phenyl group; a substituted phenyl group having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group; a heterocyclic group (the heterocyclic group herein represents a pyridyl group, a pyridin-N-oxide group, a pyrimidinyl group, a pyridazyl group, a pyrazyl group, a furyl group, a thienyl group, an oxazolyl group, an isoxazolyl group, an oxadiazolyl group, a thiazolyl group, an isothiazolyl group, an imidazolyl group, a triazolyl group, a pyrrolyl group, a pyrazolyl group or a tetrazolyl group); or a substituted heterocyclic group (which means the same as those described above) having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group or a phenyl group; and

L represents a halogen atom or a hydroxyl group).

[13] A compound represented by Formula (8):

wherein X₁a, X₂a, X₃a and X₄a each represent a hydrogen atom, a C1-C3 alkyl group, a trifluoromethyl group, a hydroxyl group, an amino group or a halogen atom;

R_(a) and R_(b) each represent a fluorine atom or a C1-C4 perfluoroalkyl group;

R_(c) represents a hydroxyl group, a group —O—R_(d) (wherein R_(d) represents a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkylsulfonyl, a C1-C3 haloalkylsulfonyl group, an arylsulfonyl group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group), a chlorine atom, a bromine atom or an iodine atom;

R₂a represents a hydrogen atom, a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group;

Y₁a and Y₅a each represent a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, a C1-C3 alkylsulfinyl group or a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a cyano group, a hydroxyl group or a halogen atom;

Y₂a and Y₄a each represent a hydrogen atom, a C1-C4 alkyl group or a halogen atom; and

G₂a represents an oxygen atom or a sulfur atom.

[14] A process for preparation of the compound represented by Formula (8) as described in [13], wherein a compound represented by Formula (9):

(wherein J represents a halogen atom or a hydroxyl group; and X₁a, X₂a, X₃a, X₄a and G₂a have the same meanings as those described in [13]),

is reacted with a compound represented by Formula (10):

(wherein R_(a), R_(b), R_(c), Y₁a, Y₂a, Y₄a, Y₅a and R₂a have the same meanings as those described in [13]).

[15] A process for preparation of a compound represented by Formula (8b):

(wherein X₁a, X₂a, X₃a, X₄a, G₂a, R₂a, Y₁a, Y₂a, Y₄a, Y₅a, R_(a) and R_(b) have the same meanings as those described in [13]; and R_(c)″ represents a chlorine atom, a bromine atom or an iodide atom);

wherein a compound represented by Formula (8a):

(wherein X₁a, X₂a, X₃a, X₄a, G₂a, R₂a, Y₁a, Y₂a, Y₄a, Y₅a, R_(a) and R_(b) have the same meanings as those described in [13]; and R_(c)′ represents a hydroxyl group or a group —O—R_(d) (wherein R_(d) represents a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, an arylsulfonyl group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group)),

is reacted with a suitable halogenating agent.

[16] A compound represented by Formula (11):

wherein X₁a, X₂a, X₃a and X₄a each represent a hydrogen atom, a C1-C3 alkyl group, a trifluoromethyl group, a hydroxyl group, an amino group or a halogen atom;

R_(a) and R_(b) each represent a fluorine atom or a C1-C4 perfluoroalkyl group;

R_(c) represents a hydroxyl group, a group —O—R_(d) (wherein R_(d) represents a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, an arylsulfonyl group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group), a chlorine atom, a bromine atom or an iodine atom;

R₁a and R₂a each represent a hydrogen atom, a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group;

Y₁a and Y₅a each represent a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a cyano group, a hydroxyl group or a halogen atom;

Y₂a and Y₄a each represent a hydrogen atom, a C1-C4 alkyl group or a halogen atom; and

G₂a represents an oxygen atom or a sulfur atom.

[17] A process for preparation of the compound represented by Formula (11) as described in [16]:

(wherein X₁a, X₂a, X₃a, X₄a, R_(a), R_(b), R_(c), R₁a, R₂a, Y₁a, Y₂a, Y₄a, Y₅a and G₂a have the same meanings as those described in [16]),

wherein the compound represented by Formula (8) as described in [13] is reacted in the presence of a suitable reducing agent.

[18] A process for preparation of a compound represented by Formula (12):

wherein X₁a, X₂a, X₃a and X₄a each represent a hydrogen atom, a C1-C3 alkyl group, a trifluoromethyl group, a hydroxyl group, an amino group or a halogen atom;

R_(a) and R_(b) each represent a fluorine atom or a C1-C4 perfluoroalkyl group;

R₁a and R₂a each represent a hydrogen atom, a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group;

Y₁a and Y₅a each represent a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a cyano group, a hydroxyl group or a halogen atom;

Y₂a and Y₄a each represent a hydrogen atom, a C1-C4 alkyl group or a halogen atom; and

G₂a represents an oxygen atom or a sulfur atom.

[19] A process for preparation of a compound represented by Formula (11b):

(wherein X₁a, X₂a, X₃a, X₄a, G₂a, R₁a, R₂a, Y₁a, Y₂a, Y₄a, Y₅a, R_(a) and R_(b) have the same meanings as those described in [18]; and R_(c)″ represents a chlorine atom, a bromine atom or an iodine atom);

wherein a compound represented by Formula (11a):

(wherein X₁a, X₂a, X₃a, X₄a, G₂a, R₁a, R₂a, Y₁a, Y₂a, Y₄a, Y₅a, R_(a) and R_(b) have the same meanings as those described in [18]; and R_(c)′ represents a hydroxyl group or a group —O—R_(d) (wherein R_(d) represents a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, an arylsulfonyl group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group)),

is reacted with a suitable halogenating agent.

[20] A compound represented by Formula (13):

wherein X₁a, X₂a, X₃a and X₄a each represent a hydrogen atom, a c1-C3 alkyl group, a trifluoromethyl group, a hydroxyl group, an amino group or a halogen atom;

R_(a) and R_(b) each represent a fluorine atom or a C1-C4 perfluoroalkyl group;

R_(c) represents a hydroxyl group, a group —O—R_(d) (wherein R_(d) represents a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, an arylsulfonyl group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group), a chlorine atom, a bromine atom or an iodine atom;

R₁a and R₂a each represent a hydrogen atom, a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group;

Y₁a and Y₅a each represent a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C4 alkylthio group, a C1-C4 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a cyano group, a hydroxyl group or a halogen atom;

Y₂a and Y₄a each represent a hydrogen atom, a C1-C4 alkyl group or a halogen atom;

G₁a and G₁a each represent an oxygen atom or a sulfur atom;

-   -   Q₁a represents a phenyl group; a substituted phenyl group having         one or more substituents, which may be identical or different,         selected from a halogen atom, a C1-C4 alkyl group, a C1-C4         haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl         group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6         cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy         group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a         C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3         haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3         haloalkylsulfonyl group, a C1-C4 alkylamino group, a         di-C1-C4-alkylamino group, a cyano group, a nitro group, a         hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4         alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an         acetylamino group and a phenyl group; a heterocyclic group (the         heterocyclic group herein represents a pyridyl group, a         pyridin-N-oxide group, a pyrimidinyl group, a pyridazyl group, a         pyrazyl group, a furyl group, a thienyl group, an oxazolyl         group, an isoxazolyl group, an oxadiazolyl group, a thiazolyl         group, an isothiazolyl group, an imidazolyl group, a triazolyl         group, a pyrrolyl group, a pyrazolyl group or a tetrazolyl         group); or a substituted heterocyclic group (which means the         same as those described above) having one or more substituents,         which may be identical or different, selected from a halogen         atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4         alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group,         a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6         halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy         group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a         C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a         C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a         C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano         group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl         group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl         group, an acetylamino group and a phenyl group.

[21] A process for preparation of the compound represented by Formula (13) as described in [20], wherein the compound represented by Formula (11) as described in [16] is reacted with a compound represented by Formula (14):

(wherein J′ represents a halogen atom or a hydroxyl group; and Q₁a and G₁a have the same meanings as those described in [20]);

or a compound represented by Formula (15):

(wherein Q₁a and G₁a have the same meanings as those described in [20]).

[22] A process for preparation of the compound represented by Formula (13) as described in [20], wherein a compound represented by Formula (16):

(wherein J″ represents a halogen atom or a hydroxyl group; and X₁a, X₂a, X₃a, X₄a, G₁a, G₂a, R₁a and Q₁a have the same meanings as those described in [20]),

is reacted with the compound represented by Formula (10) as described in [14].

[23] A process for preparation of a compound represented by Formula (17):

(wherein X₁a, X₂a, X₃a, X₄a, R_(a), R_(b), R₁a, R₂a, Y₁a, Y₂a, Y₄a, Y₅a, G₁a, G₂a and Q₁a have the same meanings as those described in [20]),

wherein the compound represented by Formula (13) as described in [20] is reacted with a suitable fluorinating agent.

[24] A process for preparation of a compound represented by Formula (13b):

(wherein X₁a, X₂a, X₃a, X₄a, R_(a), R_(b), R₁a, R₂a, Y₁a, Y₂a, Y₄a, Y₅a, G₁a, G₂a and Q₁a have the same meanings as those described in [20]; and R_(c)″ represents a chlorine atom, a bromine atom or an iodine atom),

wherein a compound represented by Formula (13a):

(wherein X₁a, X₂a, X₃a, X₄a, R_(a), R_(b), R₁a, R₂a, Y₁a, Y₂a, Y₄a, Y₅a, G₁a, G₂a and Q₁a have the same meanings as those described in [20]; and R_(c)′ represents a hydroxyl group or a group —O—R_(d) (wherein R_(d) represents a C1-C3 alkyl group, a C1-C3 haloalkyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, an arylsulfonyl group, a C1-C4 alkylcarbonyl group or a C1-C4 haloalkylcarbonyl group)),

is reacted with a suitable halogenating agent.

[25] An insecticide containing the compound as described in [1] to [8] as the active ingredient.

[26] A horticultural or agricultural insecticide containing the compound as described in [1] to [8] as an active ingredient.

[27] A method of using formulation in treating crops for cultivation or the soil to be treated with an effective amount of the compound as described in [1] to [8], in order to protect the crops from harmful organisms.

[28] A composition in which the compound as described in [1] to [8] is mixed with a suitable inert carrier, and optionally with an auxiliary agent.

[29] A mixture in which the compound as described in [1] to [8] is combined with at least one other insecticide and/or fungicide.

The compound of the present invention exhibits an excellent controlling effect as a pesticide at low doses, and also exhibits an excellent controlling effect when used in combination with a pesticide, an acaricide, a nematocide, a fungicide, a herbicide, a plant growth controlling agent, a biocide or the like.

BEST MODE FOR CARRYING OUT THE INVENTION

The terms used in the formulae described in the present invention, such as Formula (1) have the meanings as described below, respectively.

A “halogen atom” represents a fluorine atom, a chlorine atom, a bromine atom or an iodine atom.

The expression “C_(a)-C_(b) (wherein, a and b represent an integer of 1 or more)” means such that, for example, “C1-C3” means having 1 to 3 carbon atoms, “C2-C6” means having 2 to 6 carbon atoms, and “C1-C4” means having 1 to 4 carbon atoms.

The terms “n-”, “1-”, “s-” and “t-” mean normal-, iso-, secondary- and tertiary-, respectively.

The term “optionally substituted alkyl group” means a straight, branched or cyclic alkyl group substituted with substituents, which may be identical or different, such as a hydrogen atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, a C1-C6 alkylthio group, a C1-C6 haloalkylthio group, a C1-C6 alkylsulfinyl group, a C1-C6 haloalkylsulfinyl group, a C1-C6 alkylsulfonyl group, a C1-C6 haloalkylsulfonyl group, a C1-C6 alkylcarbonyl group, a C1-C6 haloalkylcarbonyl group, a C1-C6 alkoxycarbonyl group, a C1-C6 haloalkoxycarbonyl group, a C1-C6 alkylcarbonyloxy group, a C1-C6 haloalkylcarbonyloxy group, an amino group, a C1-C6 alkylamino group, a di-C1-C6-alkylamino group, an optionally substituted phenyl group, an optionally substituted phenylcarbonyl group, an optionally substituted phenylamino group and an optionally substituted heterocyclic group.

The term “optionally substituted C1-C4 alkylcarbonyl group” means a straight, branched or cyclic alkylcarbonyl group having 1 to 4 carbon atoms which is substituted with substituents, which may be identical or different, such as a hydrogen atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, a C1-C6 alkylthio group, a C1-C6 haloalkylthio group, a C1-C6 alkylsulfinyl group, a C1-C6 haloalkylsulfinyl group, a C1-C6 alkylsulfonyl group, a C1-C6 haloalkylsulfonyl group, a C1-C6 alkylcarbonyl group, a C1-C6 haloalkylcarbonyl group, a C1-C6 alkoxycarbonyl group, a C1-C6 haloalkoxycarbonyl group, a C1-C6 alkylcarbonyloxy group, a C1-C6 haloalkylcarbonyloxy group, an amino group, a C1-C6 alkylamino group, a di-C1-C6-alkylamino group, an optionally substituted phenyl group, an optionally substituted phenylcarbonyl group, an optionally substituted phenylamino group and an optionally substituted heterocyclic group.

The term “optionally substituted phenyl group” means a phenyl substituted with substituents, which may be identical or different, such as a hydrogen atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, a C1-C6 alkylthio group, a C1-C6 haloalkylthio group, a C1-C6 alkylsulfinyl group, a C1-C6 haloalkylsulfinyl group, a C1-C6 alkylsulfonyl group, a C1-C6 haloalkylsulfonyl group, a C1-C6 alkylcarbonyl group, a C1-C6 haloalkylcarbonyl group, a C1-C6 alkoxycarbonyl group, a C1-C6 haloalkoxycarbonyl group, a C1-C6 alkylcarbonyloxy group, a C1-C6 haloalkylcarbonyloxy group, an amino group, a C1-C6 alkylamino group, a di-C1-C6-alkylamino group, an acetylamino group, an optionally substituted phenyl group, an optionally substituted phenylcarbonyl group, an optionally substituted phenylamino group and an optionally substituted heterocyclic group.

The term “optionally substituted naphthyl group” means a naphthyl group substituted with substituents, which may be identical or different, such as a hydrogen atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, a C1-C6 alkylthio group, a C1-C6 haloalkylthio group, a C1-C6 alkylsulfinyl group, a C1-C6 haloalkylsulfinyl group, a C1-C6 alkylsulfonyl group, a C1-C6 haloalkylsulfonyl group, a C1-C6 alkylcarbonyl group, a C1-C6 haloalkylcarbonyl group, a C1-C6 alkoxycarbonyl group, a C1-C6 haloalkoxycarbonyl group, a C1-C6 alkylcarbonyloxy group, a C1-C6 haloalkylcarbonyloxy group, an amino group, a C1-C6 alkylamino group, a di-C1-C6-alkylamino group, an acetylamino group, an optionally substituted phenyl group, an optionally substituted phenylcarbonyl group, an optionally substituted phenylamino group and an optionally substituted heterocyclic group.

The term “optionally substituted heterocyclic group” means a heterocyclic group substituted with substituents, which may be identical or different, such as a hydrogen atom, a halogen atom, a hydroxyl group, a cyano group, a nitro group, a C1-C6 alkoxy group, a C1-C6 haloalkoxy group, a C1-C6 alkylthio group, a C1-C6 haloalkylthio group, a C1-C6 alkylsulfinyl group, a C1-C6 haloalkylsulfinyl group, a C1-C6 alkylsulfonyl group, a C1-C6 haloalkylsulfonyl group, a C1-C6 alkylcarbonyl group, a C1-C6 haloalkylcarbonyl group, a C1-C6 alkoxycarbonyl group, a C1-C6 haloalkoxycarbonyl group, a C1-C6 alkylcarbonyloxy group, a C1-C6 haloalkylcarbonyloxy group, an amino group, a C1-C6 alkylamino group, a di-C1-C6-alkylamino group, an acetylamino group, an optionally substituted phenyl group, an optionally substituted phenylcarbonyl group, an optionally substituted phenylamino group or an optionally substituted heterocyclic group.

Further, the term “C1-C3 alkyl group” represents a straight or branched alkyl group having 1 to 3 carbon atoms, such as methyl, ethyl, n-propyl, i-propyl, cyclopropyl, etc.; the term “C1-C4 alkyl group” represents a straight or branched alkyl group having 1 to 4 carbon atoms such as, for example, n-butyl, s-butyl, i-butyl, t-butyl, etc. in addition to the C1-C3 alkyl group; and the term “C1-C6 alkyl group” represents a straight or branched alkyl group having 1 to 6 carbon atoms, such as n-pentyl, 2-pentyl, 3-pentyl, neopentyl, n-hexyl, 2-hexyl, 4-methyl-2-pentyl, 3-methyl-n-pentyl, etc. in addition to the C1-C4 alkyl group.

The term “C1-C3 haloalkyl group” represents a straight or branched alkyl group having 1 to 3 carbon atoms, substituted with one or more halogen atoms which may be identical or different, such as monofluoromethyl, difluoromethyl, trifluoromethyl, monochloromethyl, dichloromethyl, trichloromethyl, monobromomethyl, dibromomethyl, tribromomethyl, 1-fluoroethyl, 2-fluoroethyl, 2,2-difluoroethyl, 2,2,2-trifluoroethyl, 1-chloroethyl, 2-chloroethyl, 2,2-dichloroethyl, 2,2,2-trichloroethyl, 1-bromoethyl, 2-bromoethyl, 2,2-dibromoethyl, 2,2,2-tribromoethyl, 2-iodoethyl, pentafluoroethyl, 3-fluoro-n-propyl, 3-chloro-n-propyl, 3-bromo-n-propyl, 1,3-difluoro-2-propyl, 1,3-dichloro-2-propyl, 1,1,1-trifluoro-2-propyl, 1-chloro-3-fluoro-2-propyl, 1,1,1,3,3,3-hexafluoro-2-propyl, 1,1,1,3,3,3-hexafluoro-2-chloro-2-propyl, 2,2,3,3,3-pentafluoro-n-propyl, heptafluoro-i-propyl or heptafluoro-n-propyl. The term “C1-C4 haloalkyl group” represents a straight or branched alkyl group having 1 to 4 carbon atoms and being substituted with one or more halogen atoms which may be identical or different, such as 4-fluoro-n-butyl, nonafluoro-n-butyl and nonafluoro-2-butyl in addition to the “C1-C3 haloalkyl group”.

The term “C2-C4 alkenyl group” represents an alkenyl group having 2 to 4 carbon atoms and a double bond in the carbon chain, such as vinyl, allyl, 2-butenyl or 3-butenyl. The Term “C2-C4 haloalkenyl group” represents a straight or branched alkenyl group having 2 to 4 carbon atoms and a double bond in the carbon chain, and being substituted with one or more halogen atoms which may be identical or different, such as 3,3-difluoro-2-propenyl, 3,3-dichloro-2-propenyl, 3,3-dibromo-2-propenyl, 2,3-dibromo-2-propenyl, 4,4-difluoro-3-butenyl and 3,4,4-tribromo-3-butenyl.

The term “C2-C4 alkynyl group” represents a straight or branched alkynyl group having 2 to 4 carbon atoms and a triple bond in the carbon chain, such as propargyl, 1-butyn-3-yl and 1-butyn-3-methyl-3-yl. The term “C2-C4 haloalkynyl group” represents a straight or branched alkenyl group having 2 to 4 carbon atoms and a triple bond in the carbon chain, and being substituted with one or more halogen atoms which may be identical or different.

The term “C3-C6 cycloalkyl group” represents a cycloalkyl group having a ring structure of 3 to 6 carbon atoms, such as cyclopropyl, cyclobutyl, cyclopentyl, 2-methylcyclopentyl, 3-methylcyclopentyl and cyclohexyl. The term “C3-C6 halocycloalkyl group” represents a cycloalkyl group having a ring structure of 3 to 6 carbon atoms and being substituted with one more halogen atoms which may be identical or different, such as 2,2,3,3-tetrafluorocyclobutyl, 2-chlorocyclohexyl and 4-chlorocyclohexyl.

The term “C1-C3 alkoxy group” represents a straight or branched alkoxy group having 1 to 3 carbon atoms, such as methoxy, ethoxy, n-propyloxy and isopropyloxy. The term “C1-C3 haloalkoxy group” represents a straight or branched haloalkoxy group having 1 to 3 carbon atoms, substituted with one or more halogen atoms which may be identical or different, such as trifluoromethoxy, 1,1,1,3,3,3-hexafluoro-2-propyloxy, 2,2,2-trifluoroethoxy, 2-chloroethoxy and 3-fluoro-n-propyloxy. The term “C1-C4 haloalkoxy group” represents a straight or branched haloalkoxy group having 1 to 4 carbon atoms and being substituted with one or more halogen atoms which may be identical or different, such as 1,1,1,3,3,4,4,4-octafluoro-2-butyloxy in addition to the “C1-C3 haloalkoxy group”.

The term “C1-C3 alkylthio group” represents a straight or branched alkylthio group having 1 to 3 carbon atoms, such as methylthio, ethylthio, n-propylthio, i-propylthio and cyclopropylthio. The term “C1-C4 alkylthio group” represents a straight or branched alkylthio group having 1 to 4 carbon atoms, such as n-butylthio, i-butylthio, s-butylthio, t-butylthio and cyclopropylmethylthio in addition to the “C1-C3 alkylthio group”. The term “C1-C3 haloalkylthio group” represents a straight or branched alkylthio group having 1 to 3 carbon atoms, substituted with one or more halogen atoms which may be identical of different, such as trifluoromethylthio, pentafluoroethylthio, 2,2,2-trifluoroethylthio, heptafluoro-n-propylthio and heptafluoro-i-propylthio. The term “C1-C4 haloalkylthio group” represents a straight or branched alkylthio group having 1 to 4 carbon atoms and being substituted with one or more halogen atoms which may be identical or different, such as nonafluoro-n-butylthio, nonafluoro-s-butylthio and 4,4,4-trifluoro-n-butylthio in addition to the “C1-C3 haloalkylthio group”.

The term “C1-C3 alkylsulfinyl group” represents a straight or branched alkylsulfinyl group having 1 to 3 carbon atoms, such as methylsulfinyl, ethylsulfinyl, n-propylsulfinyl, i-propylsulfinyl or cyclopropylsulfinyl. The term “C1-C3 haloalkylsulfinyl group” represents a straight or branched alkylsulfinyl group having 1 to 3 carbon atoms, substituted with one or more halogen atoms which may be identical or different, such as trifluoromethylsulfinyl, pentafluoroethylsulfinyl, 2,2,2-trifluoroethylsulfinyl, heptafluoro-n-propylsulfinyl and heptafluoro-i-propylsulfinyl.

The term “C1-C3 alkylsulfonyl group” represents a straight or branched alkylsulfonyl group having 1 to 3 carbon atoms, such as methylsulfonyl, ethylsulfonyl, n-propylsulfonyl, i-propylsulfonyl and cyclopropylsulfonyl. The “C1-C3 haloalkylsulfonyl group” represents a straight or branched alkylsulfonyl group having 1 to 3 carbon atoms, substituted with one or more halogen atoms which may be identical or different, such as trifluomethylsulfonyl, pentafluoroethylsulfonyl, 2,2,2-trifluoroethylsulfonyl, heptafluoro-n-propylsulfonyl or heptafluoro-i-propylsulfonyl.

The term “arylsulfonyl group” represents an arylsulfonyl group having an aromatic ring of 6 to 14 carbon atoms, such as phenylsulfonyl, p-toluenesulfonyl, 1-naphthylsulfonyl, 2-naphthylsulfonyl, anthrylsulfonyl, phenanthrylsulfonyl and acenaphthylenylsulfonyl.

The term “C1-C4 alkylamino group” represents a straight, branched or cyclic alkylamino group having 1 to 4 carbon atoms, such as methylamino, ethylamino, n-propylamino, i-propylamino, n-butylamino and cyclopropylamino. The term “di-C1-C4-alkylamino group” represents an amino group substituted with two straight or branched alkyl group having 1 to 4 carbon atoms which may be identical or different, such as dimethylamino, diethylamino and N-ethyl-N-methylamino.

The term “C1-C4 alkylcarbonyl group” represents a straight, branched or cyclic alkylcarbonyl group having 1 to 4 carbon atoms, such as formyl, acetyl, propionyl, isopropylcarbonyl and cyclopropylcarbonyl.

The term “C1-C4 haloalkylcarbonyl group” represents a straight or branched alkylcarbonyl group having 1 to 4 carbon atoms and being substituted with one or more halogen atoms which may be identical or different, such as fluoroacetyl, difluoroacetyl, trifluoroacetyl, chloroacetyl, dichloroacetyl, trichloroacetyl, bromoacetyl, iodoacetyl, 3,3,3-trifluoropropionyl and 2,2,3,3,3-pentafluoropropionyl.

The term “C1-C4 alkylcarbonyloxy group” represents a straight or branched alkylcarbonyloxy group having 1 to 4 carbon atoms, such as acetoxy and propionyloxy.

The term “C1-C4 alkoxycarbonyl group” represents a straight or branched alkoxycarbonyl group having 1 to 4 carbon atoms, such as methoxycarbonyl, ethoxycarbonyl or isopropyloxycarbonyl.

The term “C1-C4 perfluoroalkyl group” represents a straight or branched alkyl group having 1 to 4 carbon atoms and being completely substituted with fluorine atoms, such as trifluoromethyl, pentafluoroethyl, heptafluoro-n-propyl, heptafluoro-i-propyl, nonafluoro-n-butyl, nonafluoro-2-butyl and nonafluoro-i-butyl. The term “C2-C6 perfluoroakyl group”, represents a straight or branched alkyl group having 2 to 6 carbon atoms and being completely substituted with fluorine atoms, such as pentafluoroethyl, heptafluoro-n-propyl, heptafluoro-i-propyl, nonafluoro-n-butyl, nonafluoro-2-butyl, nonafluoro-i-butyl, perfluoro-n-pentyl and perfluoro-n-hexyl.

The term “C1-C6 perfluoroalkylthio group” represents a straight or branched alkylthio group having 1 to 6 carbon atoms and being completely substituted with fluorine atoms, such as trifluoromethylthio, pentafluoroethylthio, heptafluoro-n-propylthio, heptafluoro-i-propylthio, nonafluoro-n-butylthio, nonafluoro-2-butylthio, nonafluoro-i-butylthio, perfluoro-n-pentylthio and perfluoro-n-hexylthio.

The term “C1-C6 perfluoroalkylsulfinyl group” represents a straight or branched alkylsulfinyl group having 1 to 6 carbon atoms and being completely substituted with fluorine atoms, such as trifluoromethylsulfinyl, pentafluoroethylsulfinyl, heptafluoro-n-propylsulfinyl, heptafluoro-i-propylsulfinyl, nonafluoro-n-butylsulfinyl, nonafluoro-2-butylsulfinyl, nonafluoro-i-butylsulfinyl, perfluoro-n-pentylsulfinyl and perfluoro-n-hexylsulfinyl.

The term “C1-C6 perfluoroalkylsulfonyl group” represents a straight or branched alkylsulfonyl group having 1 to 6 carbon atoms and being completely substituted with fluorine atoms, such as trifluoromethylsulfonyl, pentafluoroethylsulfonyl, heptafluoro-n-propylsulfonyl, heptafluoro-i-propylsulfonyl, nonafluoro-n-butylsulfonyl, nonafluoro-2-butylsulfonyl, nonafluoro-i-butylsulfonyl, perfluoro-n-pentylsulfonyl and perfluoro-n-hexylsulfonyl.

The compound represented by Formula (1) of the invention may comprise one or a plurality of chiral carbon atoms or chiral centers in the structure, and thus two or more optical isomers may exist. The present invention includes all of the individual optical isomers and mixtures comprising them at any proportions. Furthermore, the compound represented by Formula (1) of the invention may exist in the form of two or more stereoisomers originating from carbon-carbon double bonds in the structure, and the invention includes all of the individual stereoisomers and mixtures comprising them at any proportions.

The substituents or atoms preferred as the substituents for the compounds represented by the above-mentioned formulae such as Formula (1) of the invention will be presented below.

A₁, A₂, A₃ and A₄ are preferably such that A₁ is a carbon atom, a nitrogen atom or an oxidized nitrogen atom and at the same time A₂, A₃ and A₄ are all carbon atoms, and more preferably such that A₁, A₂, A₃ and A₄ are all carbon atoms.

R₁ is preferably a hydrogen atom or a C1-C4 alkyl group, and more preferably a hydrogen atom, a methyl group or an ethyl group.

R₂ is preferably a hydrogen atom or a C1-C4 alkyl group, and more preferably a hydrogen atom, a methyl group or an ethyl group.

G₁ and G₂ are each preferably an oxygen atom or a sulfur atom, and more preferably G₁ and G₂ are both an oxygen atom.

X is preferably a hydrogen atom or a halogen atom, and more preferably a hydrogen atom or a fluorine atom.

n is preferably 0, 1 or 2, and more preferably 0 or 1.

X₁ is preferably a hydrogen atom or a halogen atom, and more preferably a hydrogen atom or a fluorine atom.

X₂ is preferably a hydrogen atom or a fluorine atom, and more preferably a hydrogen atom.

X₃ and X₄ are preferably a hydrogen atom.

Q₁ is preferably a phenyl group; a phenyl group optionally substituted with one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group and an acetylamino group; a pyridyl group; or a pyridyl group optionally substituted with one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group and an acetylamino group.

More preferably, Q₁ is a phenyl group; a phenyl group having 1 to 3 substituents, which may be identical or different, selected from a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, a trifluoromethyl group, a methoxy group, a trifluoromethoxy group, a methylthio group, a methylsulfinyl group, a methylsulfonyl group, a trifluoromethylthio group, a trifluoromethylsulfinyl group, a trifluoromethylsulfonyl group, a methylamino group, a dimethylamino group, a cyano group and a nitro group; a pyridyl group; or a pyridyl group having 1 or 2 substituents, which may be identical or different, selected from a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, a trifluoromethyl group, a methoxy group, a trifluoromethoxy group, a methylthio group, a methylsulfinyl group, a methylsulfonyl group, a trifluoromethylthio group, a trifluoromethylsulfinyl group, a trifluoromethylsulfonyl group, a methylamino group, a dimethylamino group, a cyano group and a nitro group.

Q₂ is preferably a substituted phenyl group represented by Formula (2) or a substituted pyridyl group represented by Formula (3), wherein:

Y₁ and Y₅ are each preferably a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, a 2-butyl group, a trifluoromethyl group, a methylthio group, a methylsulfinyl group, a methylsulfonyl group, a trifluoromethylthio group, a trifluoromethylsulfinyl group, a trifluoromethylsulfonyl group and a cyano group;

Y₆ and Y₉ are each preferably a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, a 2-butyl group, a trifluoromethyl group, a methylthio group, a methylsulfinyl group, a methylsulfonyl group, a trifluoromethylthio group, a trifluoromethylsulfinyl group, a trifluoromethylsulfonyl group and a cyano group;

Y₂, Y₄ and Y₇ are each preferably a hydrogen atom, a halogen atom or a methyl group, and more preferably a hydrogen atom;

Y₃ is preferably a pentafluoroethyl group, a heptafluoro-n-propyl group, a heptafluoro-i-propyl group, a nonafluoro-n-butyl group, a nonafluoro-2-butyl group, a nonafluoro-i-butyl group, a trifluoromethylthio group, a pentafluoroethylthio group, a heptafluoro-n-propylthio group, a heptafluoro-i-propylthio group, a nonafluoro-n-butylthio group, a nonafluoro-2-butylthio group, a trifluoromethylsulfinyl group, a pentafluoroethylsulfinyl group, a heptafluoro-n-propylsulfinyl group, a heptafluoro-i-propylsulfinyl group, a nonafluoro-n-butylsulfinyl group, a nonafluoro-2-butylsulfinyl group, a trifluoromethylsulfonyl group, a pentafluoroethylsulfonyl group, a heptafluoro-n-propylsulfonyl group, a heptafluoro-i-propylsulfonyl group, a nonafluoro-n-butylsulfonyl group or anonafluoro-2-butylsulfonyl group;

Y₈ is preferably a pentafluoroethyl group, a heptafluoro-n-propyl group, a heptafluoro-i-propyl group, a nonafluoro-n-butyl group, a nonafluoro-2-butyl group, a nonafluoro-i-butyl group, a trifluoromethylthio group, a pentafluoroethylthio group, a heptafluoro-n-propylthio group, a heptafluoro-i-propylthio group, a nonafluoro-n-butylthio group, a nonafluoro-2-butylthio group, a trifluoromethylsulfinyl group, a pentafluoroethylsulfinyl group, a heptafluoro-n-propylsulfinyl group, a heptafluoro-i-propylsulfinyl group, a nonafluoro-n-butylsulfinyl group, a nonafluoro-2-butylsulfinyl group, a trifluoromethylsulfonyl group, a pentafluoroethylsulfonyl group, a heptafluoro-n-propylsulfonyl group, a heptafluoro-i-propylsulfonyl group, a nonafluoro-n-butylsulfonyl group, a nonafluoro-2-butylsulfonyl group, a pentafluoroethoxy group and a 1,1,1,3,3,3-hexafluoro-i-propyloxy group.

L is preferably a chlorine atom, a bromine atom or a hydroxyl group.

R₁a is preferably a hydrogen atom or a C1-C4 alkyl group, and more preferably a hydrogen atom, a methyl group or an ethyl group.

R₂a is preferably a hydrogen atom or a C1-C4 alkyl group, and more preferably a hydrogen atom, a methyl group or an ethyl group.

G₁a and G₂a are each preferably an oxygen atom or a sulfur atom, and more preferably G_(1a) and G₂a are both an oxygen atom.

X₁a is preferably a hydrogen atom or a halogen atom, and more preferably a hydrogen atom or a fluorine atom.

X₂a is preferably a hydrogen atom or a fluorine atom, and more preferably a hydrogen atom.

X₃a and X₄a are preferably a hydrogen atom.

Y₁a and Y₅a are each preferably a chlorine atom, a bromine atom, an iodine atom, a methyl group, an ethyl group, an n-propyl group, an i-propyl group, an n-butyl group, a 2-butyl group, a trifluoromethyl group, a methylthio group, a methylsulfinyl group, a methylsulfonyl group, a trifluoromethylthio group, a trifluoromethylsulfinyl group, a trifluoromethylsulfonyl group or a cyano group.

Y₂a and Y₄a are each preferably a hydrogen atom, a halogen atom and a methyl group, and more preferably a hydrogen atom.

Q₁a is preferably a phenyl group; a phenyl group optionally substituted with one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group and an acetylamino group; a pyridyl group; or a pyridyl group optionally substituted with one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a c3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group and an acetylamino group.

More preferably, Q₁a is a phenyl group; a phenyl group having 1 to 3 substituents, which may be identical or different, selected from a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, a trifluoromethyl group, a methoxy group, a trifluoromethoxy group, a methylthio group, a methylsulfinyl group, a methylsulfonyl group, a trifluoromethylthio group, a trifluoromethylsulfinyl group, a trifluoromethylsulfonyl group, a methylamino group, a dimethylamino group, a cyano group and a nitro group; a pyridyl group; or a pyridyl group having 1 or 2 substituents, which may be identical or different, selected from a fluorine atom, a chlorine atom, a bromine atom, an iodine atom, a methyl group, a trifluoromethyl group, a methoxy group, a trifluoromethoxy group, a methylthio group, a methylsulfinyl group, a methylsulfonyl group, a trifluoromethylthio group, a trifluoromethylsulfinyl group, a trifluoromethylsulfonyl group, a methylamino group, a dimethylamino group, a cyano group and a nitro group.

R_(a) and R_(b) are each preferably a fluorine atom, a trifluoromethyl group, a pentafluoroethyl group or a heptafluoro-n-propyl group, and more preferably a fluorine atom, a trifluoromethyl group or a pentafluoroethyl group.

R_(c) is preferably a hydroxyl group, a chlorine atom, a bromine atom, an iodine atom, a methoxy group, an ethoxy group, a methylsulfonyloxy group, a trifluoromethylsulfonyloxy group, a phenylsulfonyloxy group, a p-toluenesulfonyloxy group, an acetoxy group or a trifluoroacetoxy group, and more preferably a hydroxyl group, a chlorine atom, a bromine atom, a methoxy group, a methylsulfonyloxy group, a trifluoromethylsulfonyloxy group, a phenylsulfonyloxy group or a p-toluenesulfonyloxy group, and even more preferably a hydroxyl group, a chlorine atom or a bromine atom.

R_(c)′ is preferably a hydroxyl group.

R_(c)″ is preferably a chlorine atom or a bromine atom.

J, J′ and J″ are each preferably a hydroxyl group, a chlorine atom or a bromine atom, and more preferably a chlorine atom.

Representative processes for preparation of the compound of the invention will be described in the following. Preparation of the compound of the invention is possible by following the procedure, but the preparation route is not limited only to the process for preparation described below.

With regard to the formulae prepared by the following processes for preparation, X₁, X₂, X₃, X₄, Y₁, Y₂, Y₄, Y₅, G₁, G₂, R₁, R₂ and Q₁ may correspond to X₁a, X₂a, X₃a, X₄a, Y₁a, Y₂a, Y₄a, Y₅a, G₁a, G₂a, R₁a, R₂a and Q₁a, respectively, and it is also possible vice versa. Further, Q₂ has the meaning as described in claim 1 or is represented by Formula (2):

(wherein Y₁, Y₂, Y₃, Y₄ and Y₅ have the same meanings as described above),

by Formula (3):

(wherein Y₆, Y₇, Y₈ and Y₉ have the same meanings as described above),

or by Formula (18):

(wherein Y₁a, Y₂a, Y₄a, Y₅a, R_(a), R_(b) and R_(c) have the same meaning as described above).

Preparation Process 1

wherein A₁, A₂, A₃, A₄, G₁, G₂, R₁, R₂, X, n, Q₁ and Q₂ have the same meaning as described above, and L represents a functionality capable of leaving such as a halogen atom or a hydroxyl group.

1-(i) Formula (19)+Formula (20)→Formula (21)

An aromatic carboxamide derivative having a nitro group represented by Formula (21) can be prepared by reacting an m-nitro aromatic carboxylic acid derivative having a leaving group represented by Formula (19) with an aromatic amine derivative represented by Formula (20) in a suitable solvent or without a solvent. In this step, an appropriate base can be also used.

For the solvent, use can be made of any solvent which does not impede the reaction significantly, for example, water; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform and tetrachlorocarbon; chained or cyclic ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; ketones such as acetone, methyl isobutyl ketone and cyclohexanone; amides such as dimethyl formamide and dimethyl acetamide; nitriles such as acetonitrile; and inert solvents such as 1,3-dimethyl-2-imidazolidinone, which may be used alone or in combination of two or more.

Further, for the base, use can be made of organic bases such as triethylamine, tri-n-butylamine, pyridine and 4-dimethyl aminopyridine; alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; carbonates such as sodium hydrogen carbonate and potassium carbonate; phosphates such as dipotassium hydrogen phosphate and trisodium phosphate; alkali metal hydrides such as sodium hydride; and alkali metal alcoholates such as sodium methoxide and sodium ethoxide. These bases may be appropriately used in a quantity of 0.01 to 5-fold molar equivalents with respect to the compound represented by Formula (19).

The reaction temperature may be suitably selected within the range of −20° C. to the reflux temperature of the solvent used, and the reaction time within the range of several minutes to 96 hours.

Among the compounds represented by Formula (19), an aromatic carboxylic acid halide derivative may be prepared easily from an aromatic carboxylic acid by a conventional process using a halogenating agent. A halogenating agent may be, for example, thionyl chloride, thionyl bromide, phosphorus oxychloride, oxalyl chloride, phosphorus trichloride and the like.

Meanwhile, it is possible to prepare the compound represented by Formula (21) from an m-nitro aromatic carboxylic acid derivative and the compound represented by Formula (20) without using a halogenating agent. The process is described in, for example, Chem. Ber. p. 788 (1970), in which a condensing agent comprising N,N′-dicyclohexylcarbodiimide is used, suitably with an additive such as 1-hydroxybenzotriazole. Other condensing agents that can be used in this case may include 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide, 1,1′-carbonylbis-1H-imidazole and the like.

Furthermore, for other processes for preparation of the compounds represented by Formula (21), there can be used a mixed acid anhydride process using chloroformic acid esters or a process described in J. Am. Chem. Soc., p. 5012 (1967) in order to prepare the compound represented by Formula (21). The chloroformic acid esters used in this case may include isobutyl chloroformate, isopropyl chloroformate and the like. In addition to chloroformic acid esters, diethylacetyl chloride, trimethylacetyl chloride and the like can also be used.

Both the process using a condensing agent and the mixed acid anhydride process are not limited by the solvent, the reaction temperature and the reaction time as described in the references above. An inert solvent may be used which does not impede the reaction significantly, and the reaction temperature and the reaction time may also be selected appropriately in accordance with the proceeding of the reaction.

1-(ii) Formula (21)→Formula (22)

An aromatic carboxamide derivative having an amino group represented by Formula (22) can be derived from the aromatic carboxamide derivative having a nitro group represented by Formula (21) by means of reduction. Such reduction is illustrated by a process using hydrogenation and a process using a metal compound (for example, tin(II) chloride (anhydride), iron powder, zinc powder and the like).

The reaction of the former process can be carried out in a suitable solvent in the presence of catalyst at atmospheric pressure or a higher pressure under a hydrogen atmosphere. Examples of the catalyst may include palladium catalysts such as palladium-carbon, nickel catalysts such as Raney nickel, cobalt catalysts, ruthenium catalysts, rhodium catalysts, platinum catalysts and the like, and examples of the solvent may include water; alcohols such as methanol and ethanol; aromatic hydrocarbons such as benzene, toluene; chained or cyclic ethers such as ether, dioxane, tetrahydrofuran, etc.; and esters such as ethyl acetate. The compound of Formula (22) can be efficiently prepared by appropriately selecting the pressure within a range of 0.1 to 10 Mpa, the reaction temperature within a range of −20° C. to the reflux temperature of the solvent used, and the reaction time within a range of several minutes to 96 hours.

For the latter process, there can be used a method using tin (II) chloride (anhydride) as a metal compound under the conditions described in “Organic Syntheses” Coll. Vol. III, P. 453.

1-(iii) Formula (22)+Formula (23)→Formula (24)

A compound of the invention represented by Formula (24) can be prepared by reacting the aromatic carboxamide derivative having an amino group represented by Formula (22) with the compound represented by Formula (23) in a suitable solvent. In this step, a suitable base can also be used.

For the solvent, use can be made of any solvent which does not impede the reaction significantly, for example, water; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform and tetrachlorocarbon; chained or cyclic ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; ketones such as acetone, methyl isobutyl ketone and cyclohexanone; amides such as dimethyl formamide and dimethyl acetamide; nitriles such as acetonitrile; and inert solvents such as 1,3-dimethyl-2-imidazolidinone, which may be used alone or in combination of two or more.

Further, for the base, use can be made of organic bases such as triethylamine, tri-n-butylamine, pyridine and 4-dimethyl aminopyridine; alkali metal hydroxides such as sodium hydroxide and potassium hydroxide; carbonates such as sodium hydrogen carbonate and potassium carbonate; phosphates such as dipotassium hydrogen phosphate and trisodium phosphate; alkali metal hydrides such as sodium hydride; and alkali metal alcoholates such as sodium methoxide and sodium ethoxide. Such base may be appropriately used in a quantity of 0.01 to 5-fold molar equivalents with respect to the compound represented by Formula (22). The reaction temperature may be suitably selected within the range of −20° C. to the reflux temperature of the solvent used, and the reaction time within the range of several minutes to 96 hours. It is also possible to prepare by the method using a condensing agent as described in 1-(i) or the mixed acid anhydride method.

1-(iv) Formula (24)+Formula (25)→Formula (26)

A compound represented by Formula (26) of the invention can be prepared by reacting a compound represented by Formula (24) with an alkyl compound having a leaving group represented by Formula (25) in a solvent or without a solvent. The compound represented by Formula (25) may include an alkyl halide such as methyl iodide, ethyl iodide or n-propyl bromide. Further, in this step, it is possible to use a suitable base or a solvent, and for such base or solvent, those exemplified in 1-(i) may be used. The reaction temperature, the reaction time and the like may be selected according to the examples as given in 1-(i).

Alternatively, it is also possible to prepare the compound represented by Formula (26) by reacting the compound represented by Formula (24) with an alkylating agent such as dimethyl sulfate, diethyl sulfate and the like, instead of the compound represented by Formula (25).

Preparation Process 2

wherein A₁, A₂, A₃, A₄, G₁, G₂, R₁, R₂, X, n, Q₁, Q₂, L and Hal have the same meaning as those described in the above.

2-(i) Formula (27)+Formula (23)→Formula (28)

Carboxylic acids having an acylamino group represented by Formula (28) can be prepared by reacting carboxylic acids having an amino group represented by Formula (27) as starting material with the compound represented by Formula (23) according to the conditions described in 1-(i).

2-(ii) Formula (28)→Formula (29)

A compound represented by Formula (29) can be prepared by a known conventional method in which the compound represented by Formula (28) is reacted with thionyl chloride, oxalyl chloride, phosgene, phosphorus oxychloride, phosphorus pentachloride, phosphorus trichloride, thionyl bromide, phosphorus tribromide, diethylaminosulfur trifluoride and the like.

2-(iii) Formula (29)+Formula (20)→Formula (30)

A compound represented by Formula (30) can be prepared by reacting the compound represented by Formula (29) with a compound represented by Formula (20) according to the conditions described in 1-(i).

2-(iv) Formula (28)+Formula (20)→Formula (30)

The compound represented by Formula (30) can be also prepared by reacting the compound represented by Formula (28) with the compound represented by Formula (20) according to the conditions of using a condensing agent as described in 1-(i) or the conditions of using the mixed acid anhydride method.

Preparation Process 3

wherein A₁, A₂, A₃, A₄, G₁, R₁, R₂, X, n, Q₁, Q₂ and L have the same meaning as those described in the above.

3-(i) Formula (31)→Formula (32)

A compound represented by Formula (32) can be prepared by reacting a compound represented by Formula (31) with the Lawesson's reagent according to the known conditions as described in Synthesis, p. 463 (1993) or in Synthesis, p. 829 (1984). Conditions such as a solvent, a reaction temperature and the like are not limited to those as described in the literature.

3-(ii) Formula (32)+Formula (23)→Formula (33)

A compound represented by Formula (33) can be prepared by reacting the compound represented by Formula (32) with the compound represented by Formula (23) according to the conditions as described in 1-(i).

Preparation Process 4

wherein A₁, A₂, A₃, A₄, R₁, R₂, X, n, Q₁ and Q₂ have the same meaning as those described in the above.

A compound represented by Formula (35) and a compound represented by Formula (36) can be prepared from the compound represented by Formula (34) according to the conditions as described in 3-(i). Conditions such as a solvent, a reaction temperature and the like are not limited to those as described in the literature. These two compounds can be easily separated and purified by means of a known separation and purification technique such as silica gel column chromatography.

Preparation Process 5

wherein A₁, A₂, A₃, A₄, G₁, G₂, R₁, R₂, X, n, Q₁, Q₂ and L have the same meaning as those described in the above.

5-(i) Formula (37)→Formula (38)

A compound represented by Formula (38) can be prepared by carrying out an amination reaction using ammonia according to the conditions as described in, for example, J. Org. Chem., p. 280 (1958). Conditions such as a reaction solvent are not limited to those as described in the literature, and any inert solvent which does not impede the reaction significantly may be used. A reaction temperature and a reaction time may also be selected in accordance with the proceeding of the reaction. Further, it is also possible to use methylamine, ethylamine and the like, in addition to ammonia, as the aminating agent.

5-(ii) Formula (38)+Formula (23)→Formula (39)

A compound represented by Formula (39) can be prepared by reacting the compound represented by Formula (38) with a compound represented by Formula (23) according to the conditions as described in 1-(i).

Preparation Process 6

wherein R₂ has the same meaning as described in the above; Y₁ and Y₅ each represent a methyl group, a chlorine atom, a bromine atom or an iodine atom; Y₂ and Y₄ have the same meaning as those described in the above; R_(f) represents a C1-C6 perfluoroalkyl group; and m represents 1 or 2.

6-(i) Formula (40)+Formula (41)→Formula (42)

A compound represented by Formula (42) can be prepared by reacting an aminothiophenol represented by Formula (40) with a haloalkyl iodide represented by Formula (41) according to the method as described in J. Fluorine Chem., p. 207 (1994).

The haloalkyl iodide represented by Formula (41) may include, for example, trifluoromethyl iodide, pentafluoroethyl iodide, heptafluoro-n-propyl iodide, heptafluoroisopropyl iodide, nonafluoro-n-butyl iodide, nonafluoro-2-butyl iodide and the like, and these compounds represented by Formula (40) may be suitably used in the range of 1 to 10-fold molar equivalents.

The solvent used in this step is not limited to those solvents as described in the above literature, and the solvent may be any of those not impeding the reaction significantly, for example, water; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform and tetrachlorocarbon; chained or cyclic ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; ketones such as acetone, methyl isobutyl ketone and cyclohexanone; amides such as dimethyl formamide and dimethylacetamide; nitriles such as acetonitrile; or inert solvents such as 1,3-dimethyl-2-imidazolidinone, hexamethylphosphate triamide and the like, which may used alone or in combination of two or more. A polar solvent is particularly preferred. The reaction temperature may be suitably selected within the range of −20° C. to the reflux temperature of the solvent used, and the reaction time within the range of several minutes to 96 hours.

6-(ii) Formula (42)→Formula (43)

A compound represented by Formula (43) can be prepared using a suitable halogenating agent, for example, according to the method as described in Synth. Commun., p. 1261 (1989).

The halogenating agent may include, for example, chlorine, bromine, iodine, N-chlorosuccinimide, N-bromosuccinimide, N-iodosuccinimide and the like, and these compounds represented by Formula (42) may be suitably used in the range of 1 to 10-fold molar equivalents.

In this step, it is possible to use a suitable solvent. Such solvent for use is not limited to the solvents as described in the above literature, and the solvent may be any of those not impeding the reaction significantly, for example, water; aromatic hydrocarbons such as benzene, toluene and xylene; halogenated hydrocarbons such as dichloromethane, chloroform and tetrachlorocarbon; chained or cyclic ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; ketones such as acetone, methyl isobutyl ketone and cyclohexanone; amides such as dimethyl formamide and dimethylacetamide; nitriles such as acetonitrile; or inert solvents such as 1,3-dimethyl-2-imidazolidinone, hexamethylphosphate triamide and the like, which may used alone or in combination of two or more. A polar solvent is particularly preferred. The reaction temperature may be suitably selected within the range of −20° C. to the reflux temperature of the solvent used, and the reaction time within the range of several minutes to 96 hours.

6-(iii) Formula (43)→Formula (44)

A compound represented by Formula (44) can be prepared using a suitable oxidizing agent, for example, according to the method as described in Tetrahedron Lett., p. 4955 (1994).

The oxidizing agent may include, for example, an organic peracid such as m-chloroperbenzoic acid, sodium meta-periodate, hydrogen peroxide, ozone, selenium dioxide, chromic acid, dinitrogen tetraoxide, acyl nitrate, iodine, bromine, N-bromosuccinimide, iodosyl benzyl, t-butyl hypochlorite and the like.

The solvent used in this step is not limited to the solvents described in the above literature, and the solvent may be any of those not impeding the reaction of the invention significantly. The solvent can be used alone or in combination of two or more. A polar solvent is particularly preferred. The reaction temperature may be suitably selected within the range of −20° C. to the reflux temperature of the solvent used, and the reaction time within the range of several minutes to 96 hours.

6-(iv) Formula (43)→Formula (43-2)

A compound represented by Formula (43-2), wherein either of Y₁ and Y₅ essentially represents a methyl group, can be prepared from the compound represented by Formula (43) using a suitable methylating agent. In this step, for example, the process described in Tetrahedron Lett., p. 6237 (2000) can be carried out.

6-(v) Formula (43-2)→Formula (44-2)

A compound represented by Formula (44-2), wherein either of Y₁ and Y₅ essentially represents a methyl group, can be prepared according to the process described in 6-(iii).

Further, the compound of the present invention can be prepared using the aniline derivatives represented by Formula (43), Formula (44), Formula (43-2) and Formula (44-2), by selecting a suitable production process as described in the invention.

Preparation Process 7

wherein R₂, Y₁, Y₂, Y₄, Y₅, R_(f) and m have the same meaning as those described in Preparation Process 6.

The aniline derivative represented by Formula (47) can be prepared according to Preparation Process 6 using a compound represented by Formula (45) as starting material, and further the compound of the invention can be prepared by selecting a suitable production process as described in the invention.

Preparation Process 8

wherein A₁, A₂, A₃, A₄, X, n, G₂, R₂ and Q₂ have the same meaning as those described above.

A compound represented by Formula (49) can be prepared by reacting a compound represented by Formula (48) with a suitable reacting agent in a suitable solvent using a suitable base.

For the solvent, it may be any of those which do not impede the reaction significantly, for example, aliphatic hydrocarbons such as hexane, cyclohexane and methylcyclohexane; aromatic hydrocarbons such as benzene, xylene and toluene; halogenated hydrocarbons such as dichloromethane, chloroform, tetrachlorocarbon and 1,2-dichloroethane; ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; amides such as dimethylformamide and dimethylacetamide; nitriles such as acetonitrile and propionitrile; ketones such as acetone, methyl isobutyl ketone, cyclohexanone and methyl ethyl ketone; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; 1,3-dimethyl-2-imidazolidinone, sulfolane, dimethylsulfoxide, water and the like, which can be used alone or in combination of two or more.

For the base, use can be made of, for example, organic bases such as triethylamine, tributylamine, pyridine, 4-dimethylaminopyridine; an alkali metal hydroxide such as sodium hydroxide and potassium hydroxide; a carbonate such as sodium hydrogen carbonate and potassium carbonate; a phosphate such as potassium monohydrogen phosphate, trisodium phosphate; an alkali metal hydride such as sodium hydride; an alkali metal alkoxide such as sodium methoxide, sodium ethoxide; an organic lithium such as n-butyllithium; a Grignard reagent such as ethylmagnesium bromide; and the like.

Such base can be appropriately selected or used as solvent, in the range of 0.01 to 5-fold molar equivalents with respect to the compound represented by Formula (48).

For the reacting agent, use can be made of, for example, an alkyl halide such as methyl iodide, ethyl bromide, trifluoromethyl iodide, 2,2,2-trifluoroethyl iodide; an aryl halide such as aryl iodide; a propargyl halide such as propargyl bromide; an acyl halide such as acetyl chloride; an acid anhydride such as trifluoroacetic acid anhydride; an alkyl sulfate such as dimethyl sulfate, diethyl sulfate; and the like.

Such reacting agent can be appropriately selected or used as solvent, in the range of 1 to 5-fold molar equivalents with respect to the compound represented by Formula (48).

The reaction temperature may be appropriately selected in the range from −80° C. to the reflux temperature of the solvent used, and the reaction time in the range from several minutes to 96 hours.

Preparation Process 9

wherein A₁, A₂, A₃, A₄, X, n, G₂, R₁, R₂ and Q₂ have the same meaning as those described above.

9-(i) Formula (22)→Formula (50)

A compound represented by Formula (50) can be prepared by reacting a compound represented by Formula (22) with aldehydes or ketones in a suitable solvent, and reacting under a hydrogen atmosphere in the presence of a suitable catalyst.

The solvent may be any of those which do not impede the reaction significantly, for example, aliphatic hydrocarbons such as hexane, cyclohexane and methylcyclohexane; aromatic hydrocarbons such as benzene, xylene and toluene; halogenated hydrocarbons such as dichloromethane, chloroform, tetrachlorocarbon and 1,2-dichloroethane; ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; amides such as dimethylformamide and dimethylacetamide; nitriles such as acetonitrile and propionitrile; ketones such as acetone, methyl isobutyl ketone, cyclohexanone and methyl ethyl ketone; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; 1,3-dimethyl-2-imidazolidinone, sulfolane, dimethylsulfoxide, water and the like, which can be used alone or in combination of two or more.

Examples of the catalyst may include palladium-based catalysts such as palladium-carbon, palladium hydroxide-carbon; nickel-based catalysts such as Raney nickel; cobalt catalysts, platinum catalysts, ruthenium catalysts, rhodium catalysts and the like.

Examples of the aldehydes may include, for example, formaldehyde, acetaldehyde, propionaldehyde, trifluoroacetaldehyde, difluoroacetaldehyde, fluoroacetaldehyde, chloroacetaldehyde, dichloroacetaldehyde, trichloroacetaldehyde, bromoacetaldehyde and the like.

Examples of the ketones may include, for example, acetone, perfluoroacetone, methyl ethyl ketone and the like.

The reaction pressure may be appropriately selected in the range of 1 atm to 100 atm.

The reaction temperature may be appropriately selected in the range from −20° C. to the reflux temperature of the solvent used, and the reaction time may be appropriately selected in the range from several minutes to 96 hours.

9-(ii) Formula (22)→Formula (50) (Alternative Process 1)

The compound represented by Formula (50) can be prepared by reacting the compound represented by Formula (22) with an aldehyde or a ketone in a suitable solvent, and treating the product with a suitable reducing agent.

The solvent may be any of those which do not impede the reaction significantly, for example, aliphatic hydrocarbons such as hexane, cyclohexane and methylcyclohexane; aromatic hydrocarbons such as benzene, xylene and toluene; halogenated hydrocarbons such as dichloromethane, chloroform, tetrachlorocarbon and 1,2-dichloroethane; ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; amides such as dimethylformamide and dimethylacetamide; nitriles such as acetonitrile and propionitrile; ketones such as acetone, methyl isobutyl ketone, cyclohexanone and methyl ethyl ketone; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; 1,3-dimethyl-2-imidazolidinone, sulfolane, dimethylsulfoxide, water and the like, which can be used alone or in combination of two or more.

Examples of the reducing agent may include, for example, borohydrides such as sodium borohydride, sodium cyanoborohydride, sodium triacetate borohydride and the like.

Examples of the aldehydes may include, for example, formaldehyde, acetaldehyde, propionaldehyde, trifluoroacetaldehyde, difluoroacetaldehyde, fluoroacetaldehyde, chloroacetaldehyde, dichloroacetaldehyde, trichloroacetaldehyde, bromoacetaldehyde and the like.

Examples of the ketones may include, for example, acetone, perfluoroacetone, methyl ethyl ketone and the like.

The reaction temperature may be appropriately selected in the range from −20° C. to the reflux temperature of the solvent used, and the reaction time may be appropriately selected in the range from several minutes to 96 hours.

9-(iii) Formula (22)→Formula (50) (Alternative Process 2)

The compound represented by Formula (50), wherein R₁ is methyl, can be prepared by reacting the compound represented by Formula (22) with a formylating agent in a suitable solvent or without solvent, and treating the product with a suitable reducing agent.

The solvent may be any of those which do not impede the reaction significantly, for example, aliphatic hydrocarbons such as hexane, cyclohexane and methylcyclohexane; aromatic hydrocarbons such as benzene, xylene and toluene; halogenated hydrocarbons such as dichloromethane, chloroform, tetrachlorocarbon and 1,2-dichloroethane; ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; amides such as dimethylformamide and dimethylacetamide; nitriles such as acetonitrile and propionitrile; ketones such as acetone, methyl isobutyl ketone, cyclohexanone and methyl ethyl ketone; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; 1,3-dimethyl-2-imidazolidinone, sulfolane, dimethylsulfoxide, water and the like, which can be used alone or in combination of two or more.

Examples of the formylating agent may include, for example, formaldehyde, formic acid, fluoroformic acid, formic acid anhydrides such as formyl(2,2-dimethylpropioic acid), formic acid esters such as phenyl formate, pentafluorobenzaldehyde, oxazole and the like.

Examples of the reducing agent may include, for example, inorganic acids such as sulfuric acid, organic acids such as formic acid, borohydrides such as sodium borohydride and sodium cyanoborohydride, boronic acid, lithium aluminum hydride and the like.

The reaction temperature may be appropriately selected in the range from −20° C. to the reflux temperature of the solvent used, and the reaction time may be appropriately selected in the range from several minutes to 96 hours.

Preparation Process 10

wherein X₁a, X₂a, X₃a, X₄a, Y₁a, Y₂a, Y₄a, Y₅a, G₂a, R₂a, R_(a) and R_(b) have the same meaning as those described above; R_(c)′ in Formula (51) represents a hydroxyl group or a group —O—R_(d) (wherein R_(d) has the same meaning as described above); and R_(c)″ in Formula (52) represents a chlorine atom, a bromine atom or an iodine atom.

A chlorine compound (or a bromine compound, an iodine compound) represented by Formula (52) can be prepared by reacting a compound represented by Formula (51) with a suitable halogenating agent in a suitable solvent or without a solvent. In this step, a suitable additive may also be used.

The solvent may be any of those which do not impede the reaction significantly, for example, aliphatic hydrocarbons such as hexane, cyclohexane and methylcyclohexane; aromatic hydrocarbons such as benzene, xylene and toluene; halogenated hydrocarbons such as dichloromethane, chloroform, tetrachlorocarbon and 1,2-dichloroethane; ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; amides such as dimethylformamide and dimethylacetamide; nitriles such as acetonitrile and propionitrile; ketones such as acetone, methyl isobutyl ketone and cyclohexanone; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; 1,3-dimethyl-2-imidazolidinone, sulfolane, dimethylsulfoxide, water and the like, which can be used alone or in combination of two or more.

Examples of the halogenating agent may include, for example, thionyl chloride, thionyl bromide, phosphorus oxychloride, oxalyl chloride, phosphorus trichloride, phosphorus tribromide, phosphorus pentachloride, a Rydon's reagent, sulfonyl halides such as methanesulfonyl chloride, p-toluenesulfonyl chloride and benzenesulfonyl chloride, sulfonium halide, a sulfonic acid ester, chlorine, bromine, iodine, hypohalogenic acid ester, N-halogenoamine, hydrogen chloride, hydrogen bromide, sodium bromide, potassium bromide, cyanuric chloride, 1,3-dichloro-1,2,4-triazole, titanium(IV) chloride, vanadium(IV) chloride, arsenic(III) chloride, N,N-diethyl-1,2,2-trichlorovinylamine, trichloroacetonitrile, sodium chloride, ammonium bromide, N,N-dimethylchloroforminium chloride, N,N-dimethylchloroforminium bromide, phosphorus trichloride, phosphorus tribromide, N,N-dimethylphosphoamidine dichloride and the like.

An additive may include, for example, metal salts such as zinc chloride, lithium bromide and the like, phase-transfer catalysts, organic bases such as hexamethyl phosphoric acid triamide, inorganic acids such as sulfuric acid, N,N-dimethyl formamide and the like.

Such halogenating agent may be appropriately selected or used as solvent, in the range of 0.01 to 10-fold molar equivalents with respect to the compound represented by Formula (1).

The reaction temperature may be appropriately selected in the range from −80° C. to the reflux temperature of the solvent used, and the reaction time may be appropriately selected in the range from several minutes to 96 hours.

Preparation Process 11

wherein X₁a, X₂a, X₃a, X₄a, Y₁a, Y₂a, Y₄a, Y₅a, G₂a, R₁a, R₂a, R_(a), R_(b) and R_(c) have the same meaning as those described above.

A compound represented by Formula (54) can be prepared by reacting a compound represented by Formula (53) with a suitable fluorinating agent in a suitable solvent or without a solvent.

The solvent may be any of those which do not impede the reaction significantly, for example, aliphatic hydrocarbons such as hexane, cyclohexane and methylcyclohexane; aromatic hydrocarbons such as benzene, xylene and toluene; halogenated hydrocarbons such as dichloromethane, chloroform, tetrachlorocarbon and 1,2-dichloroethane; ethers such as diethyl ether, dioxane, tetrahydrofuran and 1,2-dimethoxyethane; amides such as dimethylformamide and dimethylacetamide; nitriles such as acetonitrile and propionitrile; ketones such as acetone, methyl isobutyl ketone, cyclohexanone and methyl ethyl ketone; esters such as ethyl acetate and butyl acetate; alcohols such as methanol and ethanol; 1,3-dimethyl-2-imidazolidinone, sulfolane, dimethylsulfoxide, water and the like, which can be used alone or in combination of two or more.

Examples of the fluorinating agent may include 1,1,2,2-tetrafluoroethyl diethylamine, 2-chloro-1,1,2-trifluoroethyl diethylamine, trifluorodiphenylphospholane, difluorotriphenylphospholane, fluoroformic acid esters, sulfur tetrafluoride, potassium fluoride, potassium hydrogen fluoride, cesium fluoride, rubidium fluoride, sodium fluoride, lithium fluoride, antimony(III) fluoride, antimony(V) fluoride, zinc fluoride, cobalt fluoride, lead fluoride, copper fluoride, mercury(II) fluoride, silver fluoride, silver fluoroborate, thallium(I) fluoride, molybdenum(VI) fluoride, arsenic(III) fluoride, bromine fluoride, selenium tetrafluoride, tris(dimethylamino)sulfonium difluorotrimethylsilicate, sodium hexafluorosilicate, quaternary ammonium fluorides, (2-chloroethyl) diethylamine, diethylaminosulfur trifluoride, morpholinosulfur trifluoride, silicon tetrafluoride, hydrogen fluoride, hydrofluoric acid, hydrogen fluoride-pyridine complex, hydrogen fluoride-triethylamine complex, hydrogen fluoride salts, bis(2-methoxyethyl)amino sulfurtrifluoride, 2,2-difluoro-1,3-dimethyl-2-imidazolidinone, iodine pentafluoride, tris(diethylamino)phosphonium 2,2,3,3,4,4-hexafluorocyclobutanilide, triethylammonium hexafluorocylcobutanilide, hexafluoropropene and the like. Such fluorinating agent can be used alone or in combination of two or more. The fluorinating agent may be appropriately selected or used as solvent, in the range of 1 to 10-fold molar equivalents with respect to the compound represented by Formula (53).

Additives may be used, and examples thereof may include crown ethers such as 18-crown-6, interline transfer catalysts such as a tetraphenylphosphonium salt, inorganic salts such as calcium fluoride and calcium chloride, metal oxides such as mercury oxide, ion exchange resin and the like. Such additives can be not only added to the reaction system but also used as a pretreating agent for the fluorinating agent.

The reaction temperature may be appropriately selected in the range from −80° C. to the reflux temperature of the solvent used, and the reaction time may be appropriately selected in the range from several minutes to 96 hours.

Preparation Process 12

wherein X₁a, X₂a, X₃a, X₄a, Y₁a, Y₂a, Y₄a, Y₅a, G₂a, R₁a, R₂a, R_(a), R_(b), R_(c)′ and R_(c)″ have the same meaning as those described above.

A compound represented by Formula (56) can be prepared from the compound represented by Formula (55) according to the process described in Preparation Process 10.

Preparation Process 13

wherein X₁a, X₂a, X₃a, X₄a, Y₁a, Y₂a, Y₄a, Y₅a, G₁a, G₂a, R₁a, R₂a, R_(a), R_(b), R_(c) and Q₁a have the same meaning as those described above.

A compound represented by Formula (58) can be prepared from the compound represented by Formula (57) according to the process described in Preparation Process 11.

Preparation Process 14

wherein X₁a, X₂a, X₃a, X₄a, Y₁a, Y₂a, Y₄a, Y₅a, G₁a, G₂a, R₁a, R₂a, R_(a), R_(b), R_(c)′, R_(c)″ and Q₁a have the same meaning as those described above.

A compound represented by Formula (60) can be prepared from the compound represented by Formula (59) according to the process described in Preparation Process 10.

In all of the processes for preparation as described in the above, the desired products may be isolated from the reaction system after the reaction is completed according to conventional methods, but if required, purification can be carried out by operations such as recrystallization, column chromatography, distillation and the like. Further, the desired product can be also provided to the subsequent reaction process without being separated from the reaction system.

Hereinbelow, the representative compounds among the compounds represented by Formula (1) as the active ingredient for the insecticide of the invention will be given in Table 1 to Table 5, but the invention is not intended to be limited thereto.

In Table 6 and Table 7, the compound representative of the compound of Formula (6) will be given, but the invention is not intended to be limited thereto.

In Table 8 to Table 10, the compounds representative of the compounds of Formula (8), Formula (11) and Formula (13), but the invention is not intended to be limited thereto.

In addition, the abbreviations in the tables have the following meanings: “n-” represents normal, “Me” a methyl group, “Et” an ethyl group, “n-Pr” a normal propyl group, “i-Pr” an isopropyl group, “n-Bu” a normal butyl group, “i-Bu” an isobutyl group, “s-Bu” a secondary butyl group, “t-Bu” a tertiary butyl group, “H” a hydrogen atom, “O” an oxygen atom, “S” a sulfur atom, “C” a carbon atom, “N” a nitrogen atom, “F” a fluorine atom, “Cl” a chlorine atom, “Br’ a bromine atom, “I” an iodine atom, “CF₃” a trifluoromethyl group, “MeS” a methylthio group, “MeSO” methylsulfinyl group, “MeSO₂” a methylsulfonyl group, “MeO” a methoxy group, “NH₂” an amino group, “MeNH” a methylamino group, and “Me₂N” is a dimethylamino group; and “OH” a hydroxyl group, respectively.

TABLE 1

(X₁, X₂, X₃, X₄, R₁, R₂ = a hydrogen atom, G₁, G₂ = an oxygen atom) Comp. No. Q₁ Q₂ 1 phenyl 2,6-dimethyl-4-(pentafluoroethyl)phenyl 2 phenyl 2,6-dichloro-4-(pentafluoroethyl)phenyl 3 2-fluorophenyl 2,6-dichloro-4-(pentafluoroethyl)phenyl 4 phenyl 2,6-dibromo-4-(pentafluoroethyl)phenyl 5 2-fluorophenyl 2,6-dibromo-4-(pentafluoroethyl)phenyl 6 phenyl 2,6-dichloro-4- (heptafluoroisopropyl)phenyl 7 phenyl 2,6-dibromo-4- (heptafluoroisopropyl)phenyl 8 2-fluorophenyl 2,6-dibromo-4- (heptafluoroisopropyl)phenyl 9 phenyl 2,6-dimethyl-4-(heptafluoro-n- propyl)phenyl 10 phenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 11 2-methylphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 12 3-methylphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 13 4-methylphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 14 2-ethylphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 15 3-ethylphenyl 2,6-dimethyl-4- (heptafluorolsopropyl)phenyl 16 4-ethylphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 17 2-fluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 18 3-fluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 19 4-fluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 20 2-chlorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 21 3-chlorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 22 4-chlorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 23 2-bromophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 24 3-bromophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 25 4-bromophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 26 2-iodophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 27 3-iodophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 28 4-iodophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 29 3-cyanophenyl 2,6-dimethyl-4- (heptaflooroisopropyl)phenyl 30 4-cyanophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 31 2-nitrophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 32 3-nitrophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 33 4-nitrophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 34 2-aminophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 35 3-aminophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 36 4-aminophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 37 2-trifluoro- 2,6-dimethyl-4- methylphenyl (heptafluoroisopropyl)phenyl 38 3-trifluoro- 2,6-dimethyl-4- methylphenyl (heptafluoroisopropyl)phenyl 39 4-trifluoro- 2,6-dimethyl-4- methylphenyl (heptafluoroisopropyl)phenyl 40 2-hydroxyphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 41 2-methoxyphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 42 3-methoxyphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 43 4-methoxyphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 44 2-phenoxyphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 45 4-(1,1- 2,6-dimethyl-4- dimethylethyl)phenyl (heptafluoroisopropyl)phenyl 46 3-(dimethyl- 2,6-dimethyl-4- amino)phenyl (heptafluoroisopropyl)phenyl 47 4-(dimethyl- 2,6-dimethyl-4- amino)phenyl (heptafluoroisopropyl)phenyl 48 4-trifluoro- 2,6-dimethyl-4- methoxyphenyl (heptafluoroisopropyl)phenyl 49 2- 2,6-dimethyl-4- (acetylamino)phenyl (heptafluoroisopropyl)phenyl 50 3- 2,6-dimethyl-4- (acetylamino)phenyl (heptafluoroisopropyl)phenyl 51 4- 2,6-dimethyl-4- (acetylamino)phenyl (heptafluoroisopropyl)phenyl 52 2-acetoxyphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 53 2-(methoxy- 2,6-dimethyl-4- carbonyl)phenyl (heptafluoroisopropyl)phenyl 54 4-(methoxy- 2,6-dimethyl-4- carbonyl)phenyl (heptafluoroisopropyl)phenyl 55 2-(4-trifluoro- 2,6-dimethyl-4- methylphenyl)phenyl (heptafluoroisopropyl)phenyl 56 2,3-dimethylphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 57 2,4-dimethylphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 58 2,6-dimethylphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 59 2,3-difluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 60 2,4-difluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 61 2,5-difluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 62 2,6-difluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 63 3,4-difluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 64 3,5-difluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 65 2,3-dichlorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 66 2,4-dichlorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 67 2,5-dichlorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 68 2,6-dichlorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 69 3,4-dichlorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 70 2,4-dinitrophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 71 3,4-dinitrophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 72 2,6-dimethoxyphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 73 3,5-dimethoxyphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 74 3-methyl-4- 2,6-dimethyl-4- nitrophenyl (heptafluoroisopropyl)phenyl 75 5-amino-2- 2,6-dimethyl-4- fluorophenyl (heptafluoroisopropyl)phenyl 76 3-fluoro-2- 2,6-dimethyl-4- methylphenyl (heptafluoroisopropyl)phenyl 77 2-fluoro-5- 2,6-dimethyl-4- nitrophenyl (heptafluoroisopropyl)phenyl 78 4-fluoro-3- 2,6-dimethyl-4- nitrophenyl (heptafluoroisopropyl)phenyl 79 5-fluoro-2- 2,6-dimethyl-4- nitrophenyl (heptafluoroisopropyl)phenyl 80 2-fluoro-6- 2,6-dimethyl-4- iodophenyl (heptafluoroisopropyl)phenyl 81 2-fluoro-5-trifluoro- 2,6-dimethyl-4- methylphenyl (heptafluoroisopropyl)phenyl 82 2-chloro-4- 2,6-dimethyl-4- nitrophenyl (heptafluoroisopropyl)phenyl 83 2-chloro-4- 2,6-dimethyl-4- fluorophenyl (heptafluoroisopropyl)phenyl 84 2-chloro-6- 2,6-dimethyl-4- fluorophenyl (heptafluoroisopropyl)phenyl 85 3-chloro-4- 2,6-dimethyl-4- fluorophenyl (heptafluoroisopropyl)phenyl 86 4-chloro-2- 2,6-dimethyl-4- fluorophenyl (heptafluoroisopropyl)phenyl 87 4-chloro-2- 2,6-dimethyl-4- nitrophenyl (heptafluoroisopropyl)phenyl 88 3-methoxy-4- 2,6-dimethyl-4- nitrophenyl (heptafluoroisopropyl)phenyl 89 2-methoxy-4- 2,6-dimethyl-4- nitrophenyl (heptafluoroisopropyl)phenyl 90 2,3,4-trifluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 91 2,4,6- 2,6-dimethyl-4- trimethylphenyl (heptafluoroisopropyl)phenyl 92 2,3,6-trifluorophenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 93 2,4,5- 2,6-dimethyl-4- trimethoxyphenyl (heptafluoroisopropyl)phenyl 94 3,4,5- 2,6-dimethyl-4- trimethoxyphenyl (heptafluoroisopropyl)phenyl 95 2,3,4,5,6- 2,6-dimethyl-4- pentafluorophenyl (heptafluoroisopropyl)phenyl 96 2-biphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 97 3-biphenyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 98 1-naphthyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 99 2-naphthyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 100 pyridin-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 101 pyridin-3-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 102 pyridin-4-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 103 2-methylpyridin-5-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 104 3-methylpyridin-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 105 2-fluoropyridin-3-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 106 2-chloropyridin-3-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 107 2-chloropyridin-4-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 108 2-chloropyridin-6-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 109 2-chloropyridin-5-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 110 5-chloropyridin-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 111 4-trifluoro- 2,6-dimethyl-4- methylpyridin-3-yl (heptafluoroisopropyl)phenyl 112 3-hydroxypyridin- 2,6-dimethyl-4- 2-yl (heptafluoroisopropyl)phenyl 113 2-phenoxypyridin- 2,6-dimethyl-4- 3-yl (heptafluoroisopropyl)phenyl 114 2-methylthiopyridin- 2,6-dimethyl-4- 3-yl (heptafluoroisopropyl)phenyl 115 2,6-dimethoxy- 2,6-dimethyl-4- pyridin-3-yl (heptafluoroisopropyl)phenyl 116 2,3-dichloropyridin- 2,6-dimethyl-4- 5-yl (heptanuoroisopropyl)phenyl 117 2,5-dichloropyridin- 2,6-dimethyl-4- 3-yl (heptafluoroisopropyl)phenyl 118 2,6-dichloropyridin- 2,6-dimethyl-4- 3-yl (heptafluoroisopropyl)phenyl 119 3,5-dichloropyridin- 2,6-dimethyl-4- 4-yl (heptafluoroisopropyl)phenyl 120 (pyridine-N-oxide)- 2,6-dimethyl-4- 2-yl (heptafluoroisopropyl)phenyl 121 N-methylpyrrol-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 122 pyrazin-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 123 2-methylpyrazin-5-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 124 4-trifluoro- 2,6-dimethyl-4- methylpyrimidin-5-yl (heptafluoroisopropyl)phenyl 125 furan-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 126 furan-3-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 127 2-tetrahydrofuranyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 128 3-tetrahydrofuranyl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 129 benzofuran-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 130 tetrahydropyran-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 131 2-methyl-5,6-di- 2,6-dimethyl-4- hydro-4Hpyran-3-yl (heptafluoroisopropyl)phenyl 132 thiophen-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 133 thiophen-3-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 134 3-methylthiophen- 2,6-dimethyl-4- 2-yl (heptafluoroisopropyl)phenyl 135 2-nitrothiophen-4-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 136 2-methylthiophen- 2,6-dimethyl-4- 5-yl (heptafluoroisopropyl)phenyl 137 3-chlorothiophen- 2,6-dimethyl-4- 2-yl (heptafluoroisopropyl)phenyl 138 2-chlorothiophen- 2,6-dimethyl-4- 5-yl (heptafluoroisopropyl)phenyl 139 3-bromothiophen- 2,6-dimethyl-4- 2-yl (heptafluoroisopropyl)phenyl 140 2-bromothiophen- 2,6-dimethyl-4- 5-yl (heptafluoroisopropyl)phenyl 141 3-iodothiophen-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 142 3-phenylthlophen- 2,6-dimethyl-4- 2-yl (heptafluoroisopropyl)phenyl 143 2,4-dimethyl- 2,6-dimethyl-4- thiophen-5-yl (heptafluoroisopropyl)phenyl 144 benzothiophen-2-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 145 4-nitro-1H-pyrrol- 2,6-dimethyl-4- 2-yl (heptafluoroisopropyl)phenyl 146 3-ethyl-3H-pyrazol- 2,6-dimethyl-4- 4-yl (heptafluoroisopropyl)phenyl 147 1-methyl-3-nitro-1H- 2,6-dimethyl-4- pyrazol-4-yl (heptafluoroisopropyl)phenyl 148 3-chloro-1-methyl- 2,6-dimethyl-4- 1H-pyrazol-4-yl (heptafluoroisopropyl)phenyl 149 3-bromo-1-methyl- 2,6-dimethyl-4- 1H-pyrazol-4-yl (heptafluoroisopropyl)phenyl 150 1-methyl-3-trifluoro- 2,6-dimethyl-4- methyl-1H-pyrazol- (heptafluoroisopropyl)phenyl 4-yl 151 1-methyl-5-trifluoro- 2,6-dimethyl-4- methyl-1H-pyrazol- (heptafluoroisopropyl)phenyl 4-yl 152 isoxazol-5-yl 2,6-dimethyl-4- (heptafluoroisopropyl)phenyl 153 4-trifluoro- 2,6-dimethyl-4- methylthiazol-5-yl (heptafluoroisopropyl)phenyl 154 2,4-dimethylthiazol- 2,6-dimethyl-4- 5-yl (heptafluoroisopropyl)phenyl 155 2-ethyl-4- 2,6-dimethyl-4- methylthiazol-5-yl (heptafluoroisopropyl)phenyl 156 2-chloro-4- 2,6-dimethyl-4- methylthiazol-5-yl (heptafluoroisopropyl)phenyl 157 3-methyl-isothiazol- 2,6-dimethyl-4- 5-yl (heptafluoroisopropyl)phenyl 158 3,4-dichloro- 2,6-dimethyl-4- isothiazol-5-yl (heptafluoroisopropyl)phenyl 159 3-chlorobenzo- 2,6-dimethyl-4- thiazol-2-yl (heptafluoroisopropyl)phenyl 160 2,2-difluoro-ben- 2,6-dimethyl-4- zo[1.3]dioxol-5-yl (heptafluoroisopropyl)phenyl 161 2,2-difluoro-ben- 2,6-dimethyl-4- zo[1.3]dioxol-4-yl (heptafluoroisopropyl)phenyl 162 2-phenylquinolin- 2,6-dimethyl-4- 4-yl (heptafluoroisopropyl)phenyl 163 phenyl 2-bromo-4-(heptafluoroisopropyl)-6- methylphenyl 164 phenyl 2-ethyl-4-(heptafluoroisopropyl)-6- methylphenyl 165 2-fluorophenyl 2-ethyl-4-(heptafluoroisopropyl)-6- methylphenyl 166 phenyl 4-(heptafluoroisopropyl)-2-iodo-6- methylphenyl 167 phenyl 4-(heptafluoroisopropyl)-2-hydroxy- 6-methylphenyl 168 phenyl 2-chloro-6-ethyl-4- (heptafluoroisopropyl)phenyl 169 phenyl 2-bromo-6-ethyl-4- (heptafluoroisopropyl)phenyl 170 2-fluorophenyl 2-bromo-6-ethyl-4- (heptafluoroisopropyl)phenyl 171 phenyl 2-ethyl-4-(heptafluoroisopropyl)- 6-iodophenyl 172 2-fluorophenyl 2-ethyl-4-(heptafluoroisopropyl)- 6-iodophenyl 173 4-nitrophenyl 2-ethyl-4-(heptafluoroisopropyl)- 6-iodophenyl 174 4-cyanophenyl 2-ethyl-4-(heptafluoroisopropyl)- 6-iodophenyl 175 4-nitrophenyl 4-(heptafluoroisopropyl)-2-methyl- 6-n-propylphenyl 176 phenyl 4-(heptafluoroisopropyl)- 2-isopropyl-6-methylphenyl 177 2-fluorophenyl 4-(heptafluoroisopropyl)- 2-isopropyl-6-methylphenyl 178 phenyl 2-bromo-4-(heptafluoroisopropyl)- 6-n-propylphenyl 179 2-fluorophenyl 2-bromo-4-(heptafluoroisopropyl)- 6-n-propylphenyl 180 4-nitrophenyl 2-bromo-4-(heptafluoroisopropyl)- 6-n-propylphenyl 181 4-cyanophenyl 2-bromo-4-(heptafluoroisopropyl)- 6-n-propylphenyl 182 phenyl 4-(heptafluoroisopropyl)-2-iodo- 6-n-propylphenyl 183 2-fluorophenyl 4-(heptafluoroisopropyl)-2-iodo- 6-n-propylphenyl 184 4-nitrophenyl 4-(heptafluoroisopropyl)-2-iodo- 6-n-propylphenyl 185 4-cyanophenyl 4-(heptafluoroisopropyl)-2-iodo- 6-n-propylphenyl 186 4-trifluoro- 4-(heptafluoroisopropyl)-2-iodo- methylphenyl 6-n-propylphenyl 187 phenyl 2-chloro-4-(heptafluoroisopropyl)- 6-n-butylphenyl 188 2-fluorophenyl 2-chloro-4-(heptafluoroisopropyl)- 6-n-butylphenyl 189 phenyl 2-bromo-4-(heptafluoroisopropyl)- 6-n-butylphenyl 190 2-fluorophenyl 2-bromo-4-(heptafluoroisopropyl)- 6-n-butylphenyl 191 phenyl 4-(heptafluoroisopropyl)-2-iodo-6-n- butylphenyl 192 2-fluorophenyl 4-(heptafluoroisopropyl)-2-iodo-6-n- butylphenyl 193 phenyl 2-(2-butyl)-6-chloro-4- (heptafluoroisopropyl)phenyl 194 phenyl 2-bromo-6-(2-butyl)-4- (heptafluoroisopropyl)phenyl 195 2-fluorophenyl 2-bromo-6-(2-butyl)-4- (heptafluoroisopropyl)phenyl 196 phenyl 2-(2-butyl)-4-(heptafluoroisopropyl)-6- iodophenyl 197 2-fluorophenyl 2-bromo-6-cyano-4- (heptafluoroisopropyl)phenyl 198 phenyl 2-bromo-4-(heptafluoroisopropyl)-6- methylthiophenyl 199 2-fluorophenyl 2-bromo-4-(heptafluoroisopropyl)-6- methylthiophenyl 200 phenyl 2-bromo-4-(heptafluoroisopropyl)-6- (methylsulfinyl)phenyl 201 2-fluorophenyl 2-chloro-4-(heptafluoroisopropyl)-6- (methylsulfonyl)phenyl 202 2-chloropyridin-3-yl 2-chloro-4-(heptafluoroisopropyl)-6- (methylsulfonyl)phenyl 203 phenyl 2-bromo-4-(heptafluoroisopropyl)-6- (methylsulfonyl)phenyl 204 2-fluorophenyl 2-bromo-4-(heptafluoroisopropyl)-6- (methylsulfonyl)phenyl 205 4-fluorophenyl 2-bromo-4-(heptafluoroisopropyl)-6- (methylsulfonyl)phenyl 206 4-nitrophenyl 2-bromo-4-(heptafluoroisopropyl)-6- (methylsulfonyl)phenyl 207 4-cyanophenyl 2-bromo-4-(heptafluoroisopropyl)-6- (methylsulfonyl)phenyl 208 2-chloropyridin-3-yl 2-bromo-4-(heptafluoroisopropyl)-6- (methylsulfonyl)phenyl 209 phenyl 4-(heptafluoroisopropyl)-2- methylthiomethyl-6-trifluoromethylphenyl 210 phenyl 2-bromo-4-(heptafluoroisopropyl)-6- (trifluoromethylthio)phenyl 211 phenyl 2,6-dimethyl-4-(nonafluoro-n-butyl)phenyl 212 phenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 213 2-methylphenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 214 4-methylphenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 215 2-fluorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 216 3-fluorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 217 4-fluorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 218 2-chlorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 219 4-chlorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 220 2-bromophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 221 2-iodophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 222 3-cyanophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 223 4-cyanophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 224 2-nitrophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 225 3-nitrophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 226 4-nitrophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 227 2-trifluoro- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl methylphenyl 228 4-trifluoro- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl methylphenyl 229 4-trifluoro- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl methoxyphenyl 230 2,3-difluorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 231 2,4-difluorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 232 2,5-difluorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 233 2,6-difluorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 234 2,4-dichlorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 235 2,6-dichlorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 236 3,4-dichlorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 237 2-chloro-4- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl nitrophenyl 238 2-chloro-4- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl fluorophenyl 239 2-chloro-6- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl fluorophenyl 240 4-chloro-2- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl fluorophenyl 241 4-chloro-2- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl nitrophenyl 242 2,3,6-trifluorophenyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 243 pyridin-2-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 244 pyridin-3-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 245 2-fluoropyridin-3-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 246 2-chloropyridin-3-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 247 2-chloropyridin-5-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 248 2-methylthiopyridin- 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 3-yl 249 pyrazin-2-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 250 furan-2-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 251 furan-3-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 252 2-tetrahydrofuranyl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 253 benzofuran-2-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 254 thiophen-2-yl 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 255 2,6-difluorophenyl 2,6-dichloro-4-(trifluoromethylthio)phenyl 256 phenyl 2,6-dibromo-4-(trifluoromethylthio)phenyl 257 2,6-difluorophenyl 2,6-dibromo-4-(trifluoromethylthio)phenyl 258 phenyl 2,6-dibromo-4-(pentafluoroethylthio)phenyl 259 2-fluorophenyl 2,6-dibromo-4-(pentafluoroethylthio)phenyl 260 phenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 261 2-fluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 262 phenyl 2,6-dichloro-4-(heptafluoro-n- propylthio)phenyl 263 phenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 264 2-methylphenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 265 4-methylphenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 266 2-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 267 3-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 268 4-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 269 2-chlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 270 4-chlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 271 2-bromophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 272 2-iodophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 273 3-cyanophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 274 4-cyanophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 275 2-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 276 3-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 277 4-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 278 2-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methylphenyl propylthio)phenyl 279 4-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methylphenyl propylthio)phenyl 280 4-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methoxyphenyl propylthio)phenyl 281 2,3-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 282 2,4-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 283 2,5-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 284 2,6-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 285 3-aminophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 286 3- 2,6-dibromo-4-(heptafluoro-n- (acetylamino)phenyl propylthio)phenyl 287 3-(methylsulfonyl- 2,6-dibromo-4-(heptafluoro-n- amino)phenyl propylthio)phenyl 288 2,4-dinitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 289 3,4-dinitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 290 3-methyl-4- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylthio)phenyl 291 5-amino-2- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylthio)phenyl 292 2-fluoro-5- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylthio)phenyl 293 2-fluoro- 2,6-dibromo-4-(heptafluoro-n- 5-(methylsulfonyl- propylthio)phenyl amino)phenyl 294 2-methoxy-4- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylthio)phenyl 295 3-methoxy-4- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylthio)phenyl 296 5-(acetylamino)-2- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylthio)phenyl 297 2,4-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 298 2,6-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 299 3,4-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 300 2-chloro-4- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylthio)phenyl 301 2-chloro-4- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylthio)phenyl 302 2-chloro-6- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylthio)phenyl 303 4-chloro-2- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylthio)phenyl 304 4-chloro-2- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylthio)phenyl 305 2,3,6-trifluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 306 pyridin-2-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 307 pyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 308 2-fluoropyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 309 2-chloropyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 310 2-chloropyridin-5-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 311 2-methylthiopyridin- 2,6-dibromo-4-(heptafluoro-n- 3-yl propylthio)phenyl 312 2,6-dichloropyridin- 2,6-dibromo-4-(heptafluoro-n- 3-yl propylthio)phenyl 313 2,6-dichloropyridin- 2,6-dibromo-4-(heptafluoro-n- 4-yl propylthio)phenyl 314 2-chloro-6- 2,6-dibromo-4-(heptafluoro-n- methylpyridin-3-yl propylthio)phenyl 315 pyridin-N-oxide-2-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 316 pyrazin-2-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 317 1-methyl-3-nitro- 2,6-dibromo-4-(heptafluoro-n- 1Hpyrazol-4-yl propylthio)phenyl 318 1-methyl-3- 2,6-dibromo-4-(heptafluoro-n- trifluoromethyl- propylthio)phenyl 1Hpyrazol-4-yl 319 1-methyl-5- 2,6-dibromo-4-(heptafluoro-n- trifluoromethyl- propylthio)phenyl 1Hpyrazol-4-yl 320 2-tetrahydrofuranyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 321 2-phenylthiazol-4-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 322 furan-2-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 323 furan-3-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 324 2-tetrahydrofuranyl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 325 benzofuran-2-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 326 thiophen-2-yl 2,6-dibromo-4-(heptafluoro-n- propylthio)phenyl 327 phenyl 2,6-diiodo-4-(heptafluoro-n- propylthio)phenyl 328 2-fluorophenyl 2,6-diiodo-4-(heptafluoro-n- propylthio)phenyl 329 phenyl 2,6-dichloro-4- (heptafluoroisopropylthio)phenyl 330 2-fluorophenyl 2,6-dichloro-4- (heptafluoroisopropylthio)phenyl 331 2-chloropyridin-3-yl 2,6-dichloro-4- (heptafluoroisopropylthio)phenyl 332 phenyl 2,6-dibromo-4- (heptafluoroisopropylthio)phenyl 333 phenyl 2,6-dibromo-4-(nonafluoro-n- butylthio)phenyl 334 2-fluorophenyl 2,6-dibromo-4-(nonafluoro-n- butylthio)phenyl 335 phenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 336 2-methylphenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 337 4-methylphenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 338 2-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 339 3-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 340 4-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 341 2-chlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 342 4-chlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 343 2-bromophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 344 2-iodophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 345 3-cyanophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 346 4-cyanophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 347 2-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 348 3-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 349 4-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 350 2-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methylphenyl propylsulfinyl)phenyl 351 4-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methylphenyl propylsulfinyl)phenyl 352 4-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methoxyphenyl propylsulfinyl)phenyl 353 2,3-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 354 2,4-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 355 2,5-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 356 2,6-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 357 2,4-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 358 2,6-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 359 3,4-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 360 2-chloro-4- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylsulfinyl)phenyl 361 2-chloro-4- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylsulfinyl)phenyl 362 2-chloro-6- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylsulfinyl)phenyl 363 4-chloro-2- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylsulfinyl)phenyl 364 4-chloro-2- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylsulfinyl)phenyl 365 2,3,6-trifluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 366 pyridin-2-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 367 pyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 368 2-fluoropyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 369 2-chloropyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 370 2-chloropyridin-5-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 371 2-methylthiopyridin- 2,6-dibromo-4-(heptafluoro-n- 3-yl propylsulfinyl)phenyl 372 pyrazin-2-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 373 furan-2-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 374 thiophen-2-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfinyl)phenyl 375 2,6-difluorophenyl 2,6-dichloro-4- (trifluoromethylsulfonyl)phenyl 376 phenyl 2,6-dibromo-4- (trifluoromethylsulfonyl)phenyl 377 2,6-difluorophenyl 2,6-dibromo-4- (trifluoromethylsulfonyl)phenyl 378 2-fluorophenyl 2,6-dichloro-4- (heptafluoroisopropylsulfonyl)phenyl 379 phenyl 2,6-dichloro-4- (heptafluoroisopropylsulfonyl)phenyl 380 phenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 381 2-methylphenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 382 4-methylphenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 383 2-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 384 3-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 385 4-fluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 386 2-chlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 387 4-chlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 388 2-bromophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 389 2-iodophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 390 3-cyanophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 391 4-cyanophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 392 2-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 393 3-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 394 4-nitrophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 395 2-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methylphenyl propylsulfonyl)phenyl 396 4-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methylphenyl propylsulfonyl)phenyl 397 4-trifluoro- 2,6-dibromo-4-(heptafluoro-n- methoxyphenyl propylsulfonyl)phenyl 398 2,3-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 399 2,4-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 400 2,5-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 401 2,6-difluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 402 2,4-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 403 2,6-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 404 3,4-dichlorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 405 2-chloro-4- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylsulfonyl)phenyl 406 2-chloro-4- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylsulfonyl)phenyl 407 2-chloro-6- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylsulfonyl)phenyl 408 4-chloro-2- 2,6-dibromo-4-(heptafluoro-n- fluorophenyl propylsulfonyl)phenyl 409 4-chloro-2- 2,6-dibromo-4-(heptafluoro-n- nitrophenyl propylsulfonyl)phenyl 410 2,3,6-trifluorophenyl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 411 pyridin-2-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 412 pyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 413 2-fluoropyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 414 2-chloropyridin-3-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 415 2-chloropyridin-5-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 416 2-methylthiopyridin- 2,6-dibromo-4-(heptafluoro-n- 3-yl propylsulfonyl)phenyl 417 pyrazin-2-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 418 furan-2-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 419 thiophen-2-yl 2,6-dibromo-4-(heptafluoro-n- propylsulfonyl)phenyl 420 phenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 421 2-methylphenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 422 4-methylphenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 423 2-fluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 424 3-fluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 425 4-fluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 426 2-chlorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 427 4-chlorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 428 2-bromophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 429 2-iodophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 430 3-cyanophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 431 4-cyanophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 432 2-nitrophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 433 3-nitrophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 434 4-nitrophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 435 2-trifluoro- 2,6-dimethyl-4-(heptafluoro-n- methylphenyl propylthio)phenyl 436 4-trifluoro- 2,6-dimethyl-4-(heptafluoro-n- methylphenyl propylthio)phenyl 437 4-trifluoro- 2,6-dimethyl-4-(heptafluoro-n- methoxyphenyl propylthio)phenyl 438 2,3-difluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 439 2,4-difluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 440 2,5-difluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 441 2,6-difluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 442 2,4-dichlorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 443 2,6-dichlorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 444 3,4-dichlorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 445 2-chloro-4- 2,6-dimethyl-4-(heptafluoro-n- nitrophenyl propylthio)phenyl 446 2-chloro-4- 2,6-dimethyl-4-(heptafluoro-n- fluorophenyl propylthio)phenyl 447 2-chloro-6- 2,6-dimethyl-4-(heptafluoro-n- fluorophenyl propylthio)phenyl 448 4-chloro-2- 2,6-dimethyl-4-(heptafluoro-n- fluorophenyl propylthio)phenyl 449 4-chloro-2- 2,6-dimethyl-4-(heptafluoro-n- nitrophenyl propylthio)phenyl 450 2,3,6-trifluorophenyl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 451 pyridin-2-yl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 452 pyridin-3-yl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 453 2-fluoropyridin-3-yl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 454 2-chloropyridin-3-yl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 455 2-chloropyridin-5-yl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 456 2-methylthiopyridin- 2,6-dimethyl-4-(heptafluoro-n- 3-yl propylthio)phenyl 457 pyrazin-2-yl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 458 furan-2-yl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 459 thiophen-2-yl 2,6-dimethyl-4-(heptafluoro-n- propylthio)phenyl 460 2,6-difluorophenyl 2,6-dichloro-4- (trifluoromethylsulfonyl)phenyl 461 phenyl 2-bromo-6-(heptafluoroisopropyloxy)-4- methylpyridin-3-yl 462 2-fluorophenyl 2-bromo-6-(heptafluoroisopropyloxy)-4- methylpyridin-3-yl 463 phenyl 2,4-dimethyl-6-(2,2,2-trifluoro-1- trifluoromethylethoxy)pyridin-3-yl 464 phenyl 2-chloro-4-methyl-6-(2,2,2-trifluoro-1- trifluoromethyl-ethoxy)pyridin-3-yl 465 phenyl 2-bromo-4-methyl-6-(2,2,2-trifluoro-1- trifluoromethyl-ethoxy)pyridin-3-yl 466 2-fluorophenyl 2-bromo-4-methyl-6-(2,2,2-trifluoro-1- trifluoromethyl-ethoxy)pyridin-3-yl 467 phenyl 2-iodo-4-methyl-6-(2,2,2-trifluoro-1- trifluoromethyl-ethoxy)pyridin-3-yl

TABLE 2

(R₁, R₂ = a hydrogen atom, G₁, G₂ = an oxygen atom) Comp. No. Q₁ X₁ X₂ X₃ X₄ Q₂ 601 phenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 602 2-methylphenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 603 3-methylphenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 604 4-methylphenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 605 2-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 606 3-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 607 4-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 608 3-cyanophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 609 4-cyanophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 610 2-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 611 3-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 612 4-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 613 2-chlorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 614 4-chlorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 615 2-bromophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 616 2-iodophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 617 2-trifluoromethylphenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 618 4-trifluoromethylphenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 619 4-trifluoromethoxyphenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 620 4-(dimethylamino)phenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 621 2.3-difluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 622 2.4-difluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 623 2.5-difluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 624 2,6-difluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 625 2,4-dichlorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 626 2,6-dichlorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 627 3,4-dichlorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 628 2-fluoro-4-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 629 4-fluoro-2-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 630 2-chloro-4-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 631 4-chloro-2-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 632 2-chloro-6-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 633 2-chloro-4-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 634 4-chloro-2-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 635 2,3,6-trifluorophenyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 636 pyridin-2-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 637 pyridin-3-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 638 2-fluoropyridin-3-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 639 2-chloropyridin-3-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 640 2-chloropyridin-5-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 641 2-methylthiopyridin-3-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 642 pyrazin-2-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 643 furan-2-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 644 furan-3-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 645 2-tetrahydrofuranyl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 646 benzofuran-2-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 647 thiophen-2-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 648 2-methyl-5,6-dihydro-4H-pyran-3-yl F H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 649 phenyl H Cl H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 650 phenyl H F H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 651 4-nitrophenyl H F H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 652 4-cyanophenyl H F H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 653 2-fluorophenyl H F H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 654 4-fluorophenyl H F H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 655 4-trifluoromethylphenyl H F H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 656 2.4-difluorophenyl H F H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 657 2-chloropyridin-3-yl H F H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 658 phenyl H H CF₃ H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 659 phenyl H H H F 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 660 phenyl H H H Cl 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 661 phenyl H H H Br 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 662 phenyl H H H I 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 663 phenyl F H H F 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 664 phenyl H Br H Br 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 665 phenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 666 2-methylphenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 667 4-methylphenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 668 2-fluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 669 3-fluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 670 4-fluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 671 2-chlorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 672 4-chlorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 673 2-bromophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 674 2-iodophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 675 3-cyanophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 676 4-cyanophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 677 2-nitrophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 678 3-nitrophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 679 4-nitrophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 680 2-trifluoromethylphenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 681 4-trifluoromethylphenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 682 4-trifluoromethoxyphenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 683 2.3-difluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 684 2.4-difluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 685 2.5-difluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 686 2,6-difluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 687 2,4-dichlorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 688 2,6-dichlorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 689 3,4-dichlorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 690 2-chloro-4-nitrophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 691 2-chloro-4-fluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 692 2-chloro-6-fluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 693 4-chloro-2-fluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 694 4-chloro-2-nitrophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 695 2,3,6-trifluorophenyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 696 pyridin-2-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 697 pyridin-3-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 698 2-fluoropyridin-3-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 699 2-chloropyridin-3-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 700 2-chloropyridin-5-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 701 2-methylthiopyridin-3-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 702 pyrazin-2-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 703 furan-2-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 704 furan-3-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 705 2-tetrahydrofuranyl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 706 benzofuran-2-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 707 thiophen-2-yl F H H H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 708 phenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 709 2-methylphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 710 4-methylphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 711 2-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 712 3-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 713 4-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 714 2-chlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 715 4-chlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 716 2-bromophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 717 2-iodophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 718 3-cyanophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 719 4-cyanophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 720 2-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 721 3-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 722 4-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 723 2-trifluoromethylphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 724 4-trifluoromethylphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 725 4-trifluoromethoxyphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 726 2,3-difluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 727 2,4-difluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 728 2,5-difluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 729 2,6-difluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 730 2,4-dichlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 731 2,6-dichlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 732 3,4-dichlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 733 2-chloro-4-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 734 2-chloro-4-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 735 2-chloro-6-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 736 4-chloro-2-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 737 4-chloro-2-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 738 2,3,6-trifluorophenyl F H H H 2,6-dibromo-4-(heptafluoro -n-propylthio)phenyl 739 pyridin-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 740 pyridin-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 741 2-fluoropyridin-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 742 2-chloropyridin-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 743 2-chloropyridin-5-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 744 2-methylthiopyridin-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 745 pyrazin-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 746 furan-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 747 furan-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 748 2-tetrahydrofuranyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 749 benzofuran-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 750 thiophen-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 751 phenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 752 2-methylphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 753 4-methylphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 754 2-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 755 3-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 756 4-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 757 2-chlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 758 4-chlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 759 2-bromophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 760 2-iodophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 761 3-cyanophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 762 4-cyanophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 763 2-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 764 3-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 765 4-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 766 2-trifluoromethylphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 767 4-trifluoromethylphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 768 4-trifluoromethoxyphenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 769 2,3-difluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 770 2,4-difluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 771 2,5-difluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 772 2,6-difluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 773 2,4-dichlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 774 2,6-dichlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 775 3,4-dichlorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 776 2-chloro-4-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 777 2-chloro-4-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 778 2-chloro-6-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 779 4-chloro-2-fluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 780 4-chloro-2-nitrophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 781 2,3,6-trifluorophenyl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 782 pyridin-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 783 pyridin-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 784 2-fluoropyridin-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 785 2-chloropyridin-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 786 2-chloropyridin-5-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 787 2-methylthiopyridin-3-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 788 pyrazin-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 789 furan-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 790 thiophen-2-yl F H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 791 phenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 792 2-methylphenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 793 4-methylphenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 794 2-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 795 3-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 796 4-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 797 2-chlorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 798 4-chlorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 799 2-bromophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 800 2-iodophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 801 3-cyanophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 802 4-cyanophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 803 2-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 804 3-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 805 4-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 806 2-trifluoromethylphenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 807 4-trifluoromethylphenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 808 4-trifluoromethoxyphenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 809 2,3-difluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 810 2,4-difluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 811 2,5-difluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 812 2,6-difluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 813 2,4-dichlorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 814 2,6-dichlorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 815 3,4-dichlorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 816 2-chloro-4-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 817 2-chloro-4-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 818 2-chloro-6-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 819 4-chloro-2-fluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 820 4-chloro-2-nitrophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 821 2,3,6-trifluorophenyl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 822 pyridin-2-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 823 pyridin-3-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 824 2-fluoropyridin-3-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 825 2-chloropyridin-3-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 826 2-chloropyridin-5-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 827 2-methylthiopyridin-3-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 828 pyrazin-2-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 829 furan-2-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 830 thiophen-2-yl F H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 831 phenyl Cl H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 832 2-fluorophenyl Cl H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 833 2-chloropyridin-3-yl Cl H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl

TABLE 3

(X₃, X₄ = a hydrogen atom, G₁, G₂ = an oxygen atom) Comp. No. Q₁ R₁ R₂ X₁ X₂ Q₂ 1001 phenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1002 2-methylphenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1003 4-methylphenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1004 2-fluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1005 3-fluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1006 4-fluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1007 2-chlorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1008 4-chlorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1009 2-bromophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1010 2-iodophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1011 3-cyanophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1012 4-cyanophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1013 2-nitrophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1014 3-nitrophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1015 4-nitrophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1016 2-trifluoromethylphenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1017 4-trifluoromethylphenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1018 4-trifluoromethoxyphenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1019 2,3-difluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1020 2,4-difluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1021 2,5-difluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1022 2,6-difluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1023 2,4-dichlorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1024 2,6-dichlorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1025 3,4-dichlorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1026 2-chloro-4-nitrophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1027 2-chloro-4-fluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1028 2-chloro-6-fluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1029 4-chloro-2-fluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1030 4-chloro-2-nitrophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1031 2,3,6-trifluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1032 3-(acetylamino)phenyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1033 pyridin-2-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1034 pyridin-3-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1035 2-fluoropyridin-3-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1036 2-chloropyridin-3-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1037 2-chloropyridin-5-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1038 2-trifluoromethylpyridin-3-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1039 2-methylthiopyridin-3-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1040 pyrazin-2-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1041 furan-2-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1042 furan-3-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1043 2-tetrahydrofuranyl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1044 benzofuran-2-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1045 thiophen-2-yl Me H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1046 phenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1047 2-methylphenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1048 4-methylphenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1049 2-fluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1050 3-fluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1051 4-fluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1052 2-chlorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1053 4-chlorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1054 2-bromophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1055 2-iodophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1056 3-cyanophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1057 4-cyanophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1058 2-nitrophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1059 3-nitrophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1060 4-nitrophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1061 2-trifluoromethylphenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1062 4-trifluoromethylphenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1063 4-trifluoromethoxyphenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1064 2,3-difluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1065 2,4-difluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1066 2,5-difluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1067 2,6-difluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1068 2,4-dichlorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1069 2,6-dichlorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1070 3,4-dichlorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1071 2-chloro-4-nitrophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1072 2-chloro-4-fluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1073 2-chloro-6-fluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1074 4-chloro-2-fluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1075 4-chloro-2-nitrophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1076 2,3,6-trifluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1077 pyridin-2-yl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1078 pyridin-3-yl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1079 2-fluoropyridin-3-y1 Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1080 2-chloropyridin-3-yl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1081 2-chloropyridin-5-yl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1082 2-methylthiopyridin-3-yl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1083 pyrazin-2-yl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1084 furan-2-yl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1085 thiophen-2-yl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1086 phenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1087 2-methylphenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1088 4-methylphenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1089 2-fluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1090 3-fluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1091 4-fluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1092 2-chlorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1093 4-chlorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1094 2-bromophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1095 2-iodophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1096 3-cyanophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1097 4-cyanophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1098 2-nitrophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1099 3-nitrophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1100 4-nitrophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1101 2-trifluoromethylphenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1102 4-trifluoromethylphenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1103 4-trifluoromethoxyphenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1104 2,3-difluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1105 2,4-difluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1106 2,5-difluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1107 2,6-difluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1108 2,4-dichlorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1109 2,6-dichlorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1110 3,4-dichlorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1111 2-chloro-4-nitrophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1112 2-chloro-4-fluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1113 2-chloro-6-fluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1114 4-chloro-2-fluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1115 4-chloro-2-nitrophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1116 2,3,6-trifluorophenyl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1117 pyridin-2-yl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1118 pyridin-3-yl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1119 2-fluoropyridin-3-yl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1120 2-chloropyridin-3-yl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1121 2-chloropyridin-5-yl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1122 2-methylthiopyridin-3-yl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1123 pyrazin-2-yl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1124 furan-2-yl Me H H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1125 2-fluorophenyl Me H H H 2,6-dimethyl-4-(heptafluoro-n-propylthio)phenyl 1126 phenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1127 2-methylphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1128 4-methylphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1129 2-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1130 3-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1131 4-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1132 2-chlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1133 4-chlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1134 2-bromophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1135 2-iodophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1136 3-cyanophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1137 4-cyanophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1138 2-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1139 3-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1140 4-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1141 2-trifluoromethylphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1142 4-trifluoromethylphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1143 4-trifluoromethoxyphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1144 2,3-difluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1145 2,4-difluorophenyl Me H H H 2,6-dibromo-4-(heptaf/uoro-n-propylthio)phenyl 1146 2,5-difluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1147 2,6-difluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1148 2,4-dichlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1149 2,6-dichlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1150 3,4-dichlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1151 2-chloro-4-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1152 2-chloro-4-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1153 2-chloro-6-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1154 4-chloro-2-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1155 4-chloro-2-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1156 2,3,6-trifluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1157 pyridin-2-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1158 pyridin-3-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1159 2-fluoropyridin-3-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1160 2-chloropyridin-3-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1161 2-chloropyridin-5-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1162 2-methylthiopyridin-3-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1163 pyrazin-2-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1164 furan-2-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1165 thiophen-2-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1166 phenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1167 2-methylphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1168 4-methylphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1169 2-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1170 3-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1171 4-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1172 2-chlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1173 4-chlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1174 2-bromophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1175 2-iodophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1176 3-cyanophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1177 4-cyanophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1178 2-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1179 3-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1180 4-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1181 2-trifluoromethylphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1182 4-trifluoromethylphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1183 4-trifluoromethoxyphenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1184 2,3-difluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1185 2,4-difluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1186 2,5-difluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1187 2,6-difluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1188 2,4-dichlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1189 2,6-dichlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1190 3,4-dichlorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1191 2-chloro-4-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1192 2-chloro-4-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1193 2-chloro-6-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1194 4-chloro-2-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1195 4-chloro-2-nitrophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1196 2,3,6-trifluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1197 pyridin-2-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1198 pyridin-3-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1199 2-fluoropyridin-3-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1200 2-chloropyridin-3-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1201 2-chloropyridin-5-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1202 2-methylthiopyridin-3-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1203 pyrazin-2-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1204 furan-2-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1205 thiophen-2-yl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1206 2-fluorophenyl Et H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1207 pyridin-3-yl Et H H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1208 phenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1209 2-methylphenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1210 3-methylphenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1211 4-methylphenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1212 2-nitrophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1213 3-nitrophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1214 4-nitrophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1215 2-cyanophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1216 3-cyanophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1217 4-cyanophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1218 2-fluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1219 3-fluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1220 4-fluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1221 2-chlorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1222 4-chlorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1223 2-bromophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1224 2-iodophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1225 2-trifluoromethylphenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1226 4-trifluoromethylphenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1227 4-trifluoromethoxyphenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1228 2,3-difluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1229 2.4-difluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1230 2,5-difluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1231 2,6-difluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1232 2,4-dichlorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1233 2,6-dichlorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1234 3,4-dichlorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1235 2-fluoro-4-nitrophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1236 4-fluoro-2-nitrophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1237 2-chloro-4-fluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1238 4-chloro-2-fluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1239 2-chloro-6-fluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1240 2-chloro-4-nitrophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1241 4-chloro-2-nitrophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1242 2,3,6-trifluorophenyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1243 pyridin-2-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1244 pyridin-3-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1245 2-chloropyridin-3-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1246 2-fluoropyridin-3-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1247 2-chloropyridin-5-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1248 2-methylthiopyridin-3-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1249 pyrazin-2-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1250 furan-2-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1251 furan-3-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1252 2-tetrahydrofuranyl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1253 benzofuran-2-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1254 thiophen-2-yl Me H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1255 phenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1256 2-methylphenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1257 3-methylphenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1258 4-methylphenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1259 2-nitrophenyl Me H F H 2,6-drmethyl-4-(nonafluoro-2-butyl)phenyl 1260 3-nitrophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1261 4-nitrophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1262 2-cyanophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1263 3-cyanophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1264 4-cyanophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1265 2-fluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1266 3-fluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1267 4-fluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1268 2-chlorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1269 4-chlorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1270 2-bromophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1271 2-iodophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1272 2-trifluoromethylphenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1273 4-trifluoromethylphenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1274 4-trifluoromethoxyphenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1275 2,3-difluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1276 2.4-difluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1277 2,5-difluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1278 2,6-difluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1279 2,4-dichlorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1280 2,6-dichlorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1281 3,4-dichlorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1282 2-fluoro-4-nitrophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1283 4-fluoro-2-nitrophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1284 2-chloro-4-fluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1285 4-chloro-2-fluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1286 2-chloro-6-fluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1287 2-chloro-4-nitrophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1288 4-chloro-2-nitrophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1289 2,3,6-trifluorophenyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1290 pyridin-2-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1291 pyridin-3-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1292 2-fluoropyridin-3-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1293 2-chloropyridin-3-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1294 2-chloropyridin-5-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1295 2-methylthiopyridin-3-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1296 pyrazin-2-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1297 furan-2-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1298 furan-3-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1299 2-tetrahydrofuranyl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1300 benzofuran-2-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1301 thiophen-2-yl Me H F H 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 1302 phenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1303 2-methylphenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1304 4-methylphenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1305 2-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1306 3-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1307 4-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1308 2-chlorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1309 4-chlorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1310 2-bromophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1311 2-iodophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1312 3-cyanophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1313 4-cyanophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1314 2-nitrophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1315 3-nitrophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1316 4-nitrophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1317 2-trifluoromethylphenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1318 4-trifluoromethylphenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1319 4-trifluoromethoxyphenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1320 2,3-difluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1321 2,4-difluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1322 2,5-difluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1323 2,6-difluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1324 2,4-dichlorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1325 2,6-dichlorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1326 3,4-dichlorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1327 2-chloro-4-nitrophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1328 2-chloro-4-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1329 2-chloro-6-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1330 4-chloro-2-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1331 4-chloro-2-nitrophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1332 2,3,6-trifluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1333 pyridin-2-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1334 pyridin-3-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1335 2-fluoropyridin-3-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1336 2-chloropyridin-3-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1337 2-chloropyridin-5-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1338 2-methylthiopyridin-3-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1339 pyrazin-2-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1340 furan-2-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1341 thiophen-2-yl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1342 phenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1343 2-methylphenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1344 4-methylphenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1345 2-fluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1346 3-fluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1347 4-fluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1348 2-chlorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1349 4-chlorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1350 2-bromophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1351 2-iodophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1352 3-cyanophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1353 4-cyanophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1354 2-nitrophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1355 3-nitrophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1356 4-nitrophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1357 2-trifluoromethylphenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1358 4-trifluoromethylphenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1359 4-trifluoromethoxyphenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1360 2,3-difluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1361 2,4-difluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1362 2,5-difluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1363 2,6-difluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1364 2,4-dichlorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1365 2,6-dichlorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1366 3,4-dichlorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1367 2-chloro-4-nitrophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1368 2-chloro-4-fluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1369 2-chloro-6-fluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1370 4-chloro-2-fluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1371 4-chloro-2-nitrophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1372 2,3,6-trifluorophenyl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1373 pyridin-2-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1374 pyridin-3-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1375 2-fluoropyridin-3-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1376 2-chloropyridin-3-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1377 2-chloropyridin-5-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1378 2-methylthiopyridin-3-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1379 pyrazin-2-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1380 furan-2-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1381 thiophen-2-yl Me H F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1382 phenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1383 2-methylphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1384 4-methylphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1385 2-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1386 3-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1387 4-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1388 2-chlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1389 4-chlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1390 2-bromophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1391 2-iodophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1392 3-cyanophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1393 4-cyanophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1394 2-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1395 3-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1396 4-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1397 2-trifluoromethylphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1398 4-trifluoromethylphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1399 4-trifluoromethoxyphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1400 2,3-difluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1401 2,4-difluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1402 2,5-difluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthlo)phenyl 1403 2,6-difluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1404 2,4-dichlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1405 2,6-dichlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1406 3,4-dichlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1407 2-chloro-4-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1408 2-chloro-4-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1409 2-chloro-6-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1410 4-chloro-2-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1411 4-chloro-2-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1412 2,3,6-trifluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1413 pyridin-2-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1414 pyridin-3-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1415 2-fluoropyridin-3-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1416 2-chloropyridin-3-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1417 2-chloropyridin-5-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)pheny1 1418 2-methylthiopyridin-3-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1419 pyrazin-2-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1420 furan-2-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1421 thiophen-2-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1422 phenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1423 2-methylphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1424 4-methylphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1425 2-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1426 3-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1427 4-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1428 2-chlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1429 4-chlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1430 2-bromophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1431 2-iodophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1432 3-cyanophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1433 4-cyanophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1434 2-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1435 3-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1436 4-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1437 2-trifluoromethylphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1438 4-trifluoromethylphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1439 4-trifluoromethoxyphenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1440 2,3-difluorophenyl Me H F H 2,67dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1441 2,4-difluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1442 2,5-difluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1443 2,6-difluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1444 2,4-dichlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1445 2,6-dichlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1446 3,4-dichlorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1447 2-chloro-4-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1448 2-chloro-4-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1449 2-chloro-6-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1450 4-chloro-2-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1451 4-chloro-2-nitrophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1452 2,3,6-trifluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1453 pyridin-2-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1454 pyridin-3-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1455 2-fluoropyridin-3-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1456 2-chloropyridin-3-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1457 2-chloropyridin-5-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1458 2-methylthiopyridin-3-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1459 pyrazin-2-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1460 furan-2-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1461 thiophen-2-yl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1462 phenyl Et H F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1463 phenyl Me H H F 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1464 4-nitrophenyl Me H H F 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1465 4-cyanophenyl Me H H F 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1466 phenyl Me H H F 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1467 4-nitrophenyl Me H H F 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1468 4-cyanophenyl Me H H F 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1469 phenyl Me H H F 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1470 4-nitrophenyl Me H H F 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1471 4-cyanophenyl Me H H F 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1472 phenyl Me H H F 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1473 4-nitrophenyl Me H H F 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1474 4-cyanophenyl Me H H F 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1475 phenyl Me H H F 2,6-dibromo-4-(heptafluoro-n-propylsulfonyl)phenyl 1476 4-nitrophenyl Me H H F 2,6-dibromo-4-(heptafluoro-n-propylsulfonyl)phenyl 1477 4-cyanophenyl Me H H F 2,6-dibromo-4-(heptafluoro-n-propylsulfonyl)phenyl 1478 phenyl H Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1479 phenyl H Me H H 2-bromo-4-(heptafluoroisopropyl)-6-methylphenyl 1480 phenyl H Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1481 2-fluorophenyl H Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1482 phenyl H Et H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1483 phenyl H i-Pr H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1484 phenyl H acetyl H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1485 phenyl H Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1486 2-fluorophenyl H Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1487 phenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1488 2-methylphenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1489 4-methylphenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1490 2-fluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1491 3-fluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1492 4-fluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1493 2-chlorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1494 4-chlorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1495 2-bromophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1496 2-iodophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1497 3-cyanophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1498 4-cyanophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1499 2-nitrophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1500 3-nitrophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1501 4-nitrophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1502 2-trifluoromethy1phenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1503 4-trifluoromethylphenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1504 4-trifluoromethoxyphenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1505 2,3-difluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1506 2,4-difluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1507 2,5-difluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1508 2,6-difluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1509 2,4-dichlorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1510 2,6-dichlorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1511 3,4-dichlorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1512 2-chloro-4-nitrophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1513 2-chloro-4-fluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1514 2-chloro-6-fluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1515 4-chloro-2-fluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1516 4-chloro-2-nitrophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1517 2,3,6-trifluorophenyl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1518 pyridin-2-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1519 pyridin-3-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1520 2-fluoropyridin-3-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1521 2-chloropyridin-3-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1522 2-chloropyridin-5-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1523 2-methylthiopyridin-3-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1524 pyrazin-2-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1525 furan-2-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1526 thiophen-2-yl Me Me H H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1527 phenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1528 2-methylphenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1529 4-methylphenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1530 2-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1531 3-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1532 4-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1533 2-chlorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1534 4-chlorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1535 2-bromophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1536 2-iodophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1537 3-cyanophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1538 4-cyanophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1539 2-nitrophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1540 3-nitrophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1541 4-nitrophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1542 2-trifluoromethylphenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1543 4-trifluoromethylphenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1544 4-trifluoromethoxyphenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1545 2,3-difluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1546 2,4-difluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1547 2,5-difluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1548 2,6-difluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1549 2,4-dichlorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1550 2,6-dichlorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1551 3,4-dichlorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1552 2-chloro-4-nitrophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1553 2-chloro-4-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1554 2-chloro-6-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1555 4-chloro-2-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1556 4-chloro-2-nitrophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1557 2,3,6-trifluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1558 pyridin-2-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1559 pyridin-3-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1560 2-fluoropyridin-3-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1561 2-chloropyridin-3-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1562 2-chloropyridin-5-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1563 2-methylthiopyridin-3-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1564 pyrazin-2-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1565 furan-2-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1566 thiophen-2-yl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1567 phenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1568 2-methylphenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1569 4-methylphenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1570 2-fluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1571 3-fluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1572 4-fluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1573 2-chlorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1574 4-chlorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1575 2-bromophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1576 2-iodophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1577 3-cyanophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1578 4-cyanophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1579 2-nitrophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1580 3-nitrophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1581 4-nitrophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1582 2-trifluoromethylphenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1583 4-trifluoromethylphenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1584 4-trifluoromethoxyphenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1585 2,3-difluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1586 2,4-difluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1587 2,5-difluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1588 2,6-difluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1589 2,4-dichlorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1590 2,6-dichlorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1591 3,4-dichlorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1592 2-chloro-4-nitrophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1593 2-chloro-4-fluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1594 2-chloro-6-fluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1595 4-chloro-2-fluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1596 4-chloro-2-nitrophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1597 2,3,6-trifluorophenyl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1598 pyridin-2-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1599 pyridin-3-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1600 2-fluoropyridin-3-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1601 2-chloropyridin-3-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1602 2-chloropyridin-5-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1603 2-methylthiopyridin-3-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1604 pyrazin-2-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1605 furan-2-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1606 thiophen-2-yl Me Me H H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1607 phenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1608 2-methylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1609 3-methylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1610 4-methylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1611 2-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1612 3-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1613 4-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1614 2-cyanophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1615 3-cyanophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1616 4-cyanophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1617 2-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1618 3-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1619 4-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1620 2-chlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1621 4-chlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1622 2-bromophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1623 2-iodophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1624 2-trifluoromethylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1625 4-trifluoromethylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1626 4-trifluoromethoxyphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1627 2,3-difluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1628 2.4-difluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1629 2,5-difluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1630 2,6-difluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1631 2,4-dichlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1632 2,6-dichlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1633 3,4-dichlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1634 2-fluoro-4-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1635 4-fluoro-2-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1636 2-chloro-4-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1637 4-chloro-2-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1638 2-chloro-6-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1639 2-chloro-4-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1640 4-chloro-2-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1641 2,3,6-trifluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1642 pyridin-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1643 pyridin-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1644 2-fluoropyridin-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1645 2-chloropyridin-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1646 2-chloropyridin-5-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1647 2-methylthiopyridin-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1648 pyrazin-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1649 furan-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1650 furan-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1651 2-tetrahydrofuranyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1652 benzofuran-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1653 thiophen-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1654 3,4-dinitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1655 3-methoxy-4-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1656 2,3,4-trifluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1657 phenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1658 2-methylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1659 4-methylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1660 2-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1661 3-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1662 4-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1663 2-chlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1664 4-chlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1665 2-bromophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1666 2-iodophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1667 3-cyanophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1668 4-cyanophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1669 2-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1670 3-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1671 4-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1672 2-trifluoromethylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1673 4-trifluoromethylphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1674 4-trifluoromethoxyphenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1675 2,3-difluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1676 2,4-difluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1677 2,5-difluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1678 2,6-difluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1679 2,4-dichlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1680 2,6-dichlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1681 3,4-dichlorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1682 2-chloro-4-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1683 2-chloro-4-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1684 2-chloro-6-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1685 4-chloro-2-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1686 4-chloro-2-nitrophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1687 2,3,6-trifluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1688 pyridin-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1689 pyridin-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1690 2-fluoropyridin-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1691 2-chloropyridin-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1692 2-chloropyridin-5-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1693 2-methylthiopyridin-3-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1694 pyrazin-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1695 furan-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1696 thiophen-2-yl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1697 phenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1698 2-methylphenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1699 4-methylphenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1700 2-fluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1701 3-fluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1702 4-fluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1703 2-chlorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1704 4-chlorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1705 2-bromophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1706 2-iodophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1707 3-cyanophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1708 4-cyanophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1709 2-nitrophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1710 3-nitrophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1711 4-nitrophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1712 2-trifluoromethylphenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1713 4-trifluoromethylphenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1714 4-trifluoromethoxyphenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1715 2,3-difluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1716 2,4-difluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1717 2,5-difluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1718 2,6-difluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1719 2,4-dichlorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1720 2,6-dichlorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1721 3,4-dichlorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1722 2-chloro-4-nitrophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1723 2-chloro-4-fluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1724 2-chloro-6-fluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1725 4-chloro-2-fluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1726 4-chloro-2-nitrophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1727 2,3,6-trifluorophenyl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1728 pyridin-2-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1729 pyridin-3-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1730 2-fluoropyridin-3-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1731 2-chloropyridin-3-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1732 2-chloropyridin-5-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1733 2-methylthiopyridin-3-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1734 pyrazin-2-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1735 furan-2-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1736 thiophen-2-yl Me Me F H 2,6-dimethyl-4-(heptafluoroisopropyl)phenyl 1737 phenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1738 2-methylphenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1739 4-methylphenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1740 2-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1741 3-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1742 4-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1743 2-chlorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1744 4-chlorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1745 2-bromophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1746 2-iodophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1747 3-cyanophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1748 4-cyanophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1749 2-nitrophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1750 3-nitrophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1751 4-nitrophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1752 2-trifluoromethylphenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1753 4-trifluoromethylphenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1754 4-trifluoromethoxyphenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1755 2,3-difluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methy1sulfonyl)phenyl 1756 2,4-difluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1757 2,5-difluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1758 2,6-difluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1759 2,4-dichlorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1760 2,6-dichlorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1761 3,4-dichlorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1762 2-chloro-4-nitrophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1763 2-chloro-4-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1764 2-chloro-6-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1765 4-chloro-2-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1766 4-chloro-2-nitrophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1767 2,3,6-trifluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1768 pyridin-2-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1769 pyridin-3-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1770 2-fluoropyridin-3-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1771 2-chloropyridin-3-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1772 2-chloropyridin-5-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1773 2-methylthiopyridin-3-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1774 pyrazin-2-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1775 furan-2-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1776 thiophen-2-yl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl)phenyl 1777 phenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1778 2-methylphenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1779 4-methylphenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1780 2-fluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1781 3-fluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1782 4-fluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1783 2-chlorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1784 4-chlorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1785 2-bromophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1786 2-iodophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1787 3-cyanophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1788 4-cyanophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1789 2-nitrophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1790 3-nitrophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1791 4-nitrophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1792 2-trifluoromethylphenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1793 4-trifluoromethylphenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1794 4-trifluoromethoxyphenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1795 2,3-difluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1796 2,4-difluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1797 2,5-difluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1798 2,6-difluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1799 2,4-dichlorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1800 2,6-dichlorophenyl Me He F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1801 3,4-dichlorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1802 2-chloro-4-nitrophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1803 2-chloro-4-fluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1804 2-chloro-6-fluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1805 4-chloro-2-fluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1806 4-chloro-2-nitrophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1807 2,3,6-trifluorophenyl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1808 pyridin-2-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1809 pyridin-3-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1810 2-fluoropyridin-3-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1811 2-chloropyridin-3-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1812 2-chloropyridin-5-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1813 2-methylthiopyridin-3-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1814 pyrazin-2-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1815 furan-2-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1816 thiophen-2-yl Me Me F H 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 1817 phenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1818 2-methylphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1819 4-methylphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1820 2-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1821 3-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1822 4-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1823 2-chlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1824 4-chlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1825 2-bromophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1826 2-iodophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1827 3-cyanophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1828 4-cyanophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1829 2-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1830 3-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1831 4-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1832 2-trifluoromethylphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1833 4-trifluoromethylphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1834 4-trifluoromethoxyphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1835 2,3-difluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1836 2,4-difluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1837 2,5-difluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1838 2,6-difluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1839 2,4-dichlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1840 2,6-dichlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1841 3,4-dichlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1842 2-chloro-4-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1843 2-chloro-4-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1844 2-chloro-6-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1845 4-chloro-2-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1846 4-chloro-2-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1847 2,3,6-trifluorophenyl Me Me F H 2,6-dibromo-4-(heptaflnoro-n-propylthio)phenyl 1848 pyridin-2-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1849 pyridin-3-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1850 2-fluoropyridin-3-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1851 2-chloropyridin-3-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1852 2-chloropyridin-5-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1853 2-methylthiopyridin-3-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1854 pyrazin-2-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1855 furan-2-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1856 thiophen-2-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 1857 phenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1858 2-methylphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1859 4-methylphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1860 2-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1861 3-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1862 4-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1863 2-chlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1864 4-chlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1865 2-bromophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1866 2-iodophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1867 3-cyanophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1868 4-cyanophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1869 2-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1870 3-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1871 4-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1872 2-trifluoromethylphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1873 4-trifluoromethylphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1874 4-trifluoromethoxyphenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1875 2,3-difluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1876 2,4-difluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1877 2,5-difluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1878 2,6-difluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1879 2,4-dichlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1880 2,6-dichlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1881 3,4-dichlorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1882 2-chloro-4-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1883 2-chloro-4-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1884 2-chloro-6-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1885 4-chloro-2-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1886 4-chloro-2-nitrophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1887 2,3,6-trifluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1888 pyridin-2-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1889 pyridin-3-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1890 2-fluoropyridin-3-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1891 2-chloropyridin-3-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1892 2-chloropyridin-5-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1893 2-methylthiopyridin-3-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1894 pyrazin-2-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1895 furan-2-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1896 thiophen-2-yl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 1897 2-fluorophenyl Me H H H 2,6-dibromo-4-(pentafluoroethyl)phenyl 1898 2-fluorophenyl Me H H H 2-bromo-4-heptafluoroisopropyl)-6-methylphenyl 1899 2-fluorophenyl Me H H H 2-ethyl-4-(heptafluoroisopropyl)-6-methylphenyl 1900 2-fluorophenyl Me H H H 4-(heptafluoroisopropyl)-2-iodo-6-methylphenyl 1901 2-fluorophenyl Me H H H 2-chloro-6-ethyl-4-(heptafluoroisopropyl)phenyl 1902 2-fluorophenyl Me H H H 2-bromo-6-ethyl-4-(heptafluoroisopropyl)phenyl 1903 2-fluorophenyl Me H H H 2-ethyl-4-(heptafluoroisopropyl)-6-iodophenyl 1904 2-fluorophenyl Me H H H 4-(heptafluoroisopropyl)-2-isopropyl-6-methylphenyl 1905 2-fluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-n-propylphenyl 1906 2-fluorophenyl Me H H H 2-bromo-4-(heptafluoroisopropyl)-6-(trifluoromethylthio)phenyl 1907 2-fluorophenyl Me H H H 2,6-dibromo-4-(trifluoromethylthio)phenyl 1908 2-fluorophenyl Me H H H 2,6-dibromo-4-(pentafluoroethylthio)phenyl 1909 2-fluorophenyl Me H H H 2,6-dibromo-4-(nonafluoro-n-butylthio)phenyl 1910 2-fluorophenyl Me H H H 2,6-dichloro-4-(heptafluoroisopropylsulfonyl)phenyl 1911 2-fluorophenyl Me H H H 2,6-dibromo-4-(heptafluoro-n-propylsulfonyl)phenyl 1912 2-fluorophenyl Me H H H 2-bromo-6-(heptafluoroisopropyloxy)-4-methylpyridin-3-yl 1913 2-fluorophenyl Me H H H 2,4-dimethyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1914 2-fluorophenyl Me H H H 2-chloro-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1915 2-fluorophenyl Me H H H 2-bromo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1916 2-fluorophenyl Me H H H 2-iodo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1917 2-fluorophenyl Me H F H 2,6-dibromo-4-(pentafluoroethyl)phenyl 1918 2-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-methylphenyl 1919 2-fluorophenyl Me H F H 2-ethyl-4-(heptafluoroisopropyl)-6-methylphenyl 1920 2-fluorophenyl Me H F H 4-(heptafluoroisopropyl)-2-iodo-6-methylphenyl 1921 2-fluorophenyl Me H F H 2-chloro-6-ethyl-4-(heptafluoroisopropyl)phenyl 1922 2-fluorophenyl Me H F H 2-bromo-6-ethyl-4-(heptafluoroisopropyl)phenyl 1923 2-fluorophenyl Me H F H 2-ethyl-4-(heptafluoroisopropyl)-6-iodophenyl 1924 2-fluorophenyl Me H F H 4-(heptafluoroisopropyl)-2-isopropyl-6-methylphenyl 1925 2-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-n-propylphenyl 1926 2-fluorophenyl Me H F H 2-bromo-4-(heptafluoroisopropyl)-6-(trifluoromethylthio)phenyl 1927 2-fluorophenyl Me H F H 2,6-dibromo-4-(trifluoromethylthio)phenyl 1928 2-fluorophenyl Me H F H 2,6-dibromo-4-(pentafluoroethylthio)phenyl 1929 2-fluorophenyl Me H F H 2,6-dibromo-4-(nonafluoro-n-butylthio)phenyl 1930 2-fluorophenyl Me H F H 2,6-dichloro-4-(heptafluoroisopropylsulfonyl)phenyl 1931 2-fluorophenyl Me H F H 2,6-dibromo-4-(heptafluoro-n-propylsulfonyl)phenyl 1932 2-fluorophenyl Me H F H 2-bromo-6-(heptafluoroisopropyloxy)-4-methylpyridin-3-yl 1933 2-fluorophenyl Me H F H 2,4-dimethyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1934 2-fluorophenyl Me H F H 2-chloro-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1935 2-fluorophenyl Me H F H 2-bromo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1936 2-fluorophenyl Me H F H 2-iodo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1937 2-fluorophenyl Me Me H H 2,6-dibromo-4-(pentafluoroethyl)phenyl 1938 2-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-methylphenyl 1939 2-fluorophenyl Me Me H H 2-ethyl-4-(heptafluoroisopropyl)-6-methylphenyl 1940 2-fluorophenyl Me Me H H 4-(heptafluoroisopropyl)-2-iodo-6-methylphenyl 1941 2-fluorophenyl Me Me H H 2-chloro-6-ethyl-4-(heptafluoroisopropyl) phenyl 1942 2-fluorophenyl Me Me H H 2-bromo-6-ethyl-4-(heptafluoroisopropyl)phenyl 1943 2-fluorophenyl Me Me H H 2-ethyl-4-(heptafluoroisopropyl)-6-iodophenyl 1944 2-fluorophenyl Me Me H H 4-(heptafluoroisopropyl)-2-isopropyl-6-methylphenyl 1945 2-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-n-propylphenyl 1946 2-fluorophenyl Me Me H H 2-bromo-4-(heptafluoroisopropyl)-6-(trifluoromethylthio)phenyl 1947 2-fluorophenyl Me Me H H 2,6-dibromo-4-(trif1uoromethylthio)phenyl 1948 2-fluorophenyl Me Me H H 2,6-dibromo-4-(pentafluoroethylthio)phenyl 1949 2-fluorophenyl Me Me H H 2,6-dibromo-4-(nonafluoro-n-butylthio)phenyl 1950 2-fluorophenyl Me Me H H 2,6-dichloro-4-(heptafluoroisopropylsulfonyl)phenyl 1951 2-fluorophenyl Me Me H H 2,6-dibromo-4-(heptafluoro-n-propylsulfonyl)phenyl 1952 2-fluorophenyl Me Me H H 2-bromo-6-(heptafluoroisopropyloxy)-4-methylpyridin-3-yl 1953 2-fluorophenyl Me Me H H 2,4-dimethyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1954 2-fluorophenyl Me Me H H 2-chloro-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1955 2-fluorophenyl Me Me H H 2-bromo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1956 2-fluorophenyl Me Me H H 2-iodo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1957 2-fluorophenyl Me Me F H 2,6-dibromo-4-(pentafluoroethyl)phenyl 1958 2-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-methylphenyl 1959 2-fluorophenyl Me Me F H 2-ethy1-4-(heptafluoroisopropyl)-6-methylphenyl 1960 2-fluorophenyl Me Me F H 4-(heptafluoroisopropyl)-2-iodo-6-methylphenyl 1961 2-fluorophenyl Me Me F H 2-chloro-6-ethyl-4-(heptafluoroisopropyl)phenyl 1962 2-fluorophenyl Me Me F H 2-bromo-6-ethyl-4-(heptafluoroisopropyl) phenyl 1963 2-fluorophenyl Me Me F H 2-ethyl-4-(heptafluoroisopropyl-6-iodophenyl 1964 2-fluorophenyl Me Me F H 4-(heptafluoroisopropyl)-2-isopropyl-6-methylphenyl 1965 2-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-n-propylphenyl 1966 2-fluorophenyl Me Me F H 2-bromo-4-(heptafluoroisopropyl)-6-(trifluoromethylthio)phenyl 1967 2-fluorophenyl Me Me F H 2,6-dibromo-4-(trifluoromethylthio)phenyl 1968 2-fluorophenyl Me Me F H 2,6-dibromo-4-(pentafluoroethylthio)phenyl 1969 2-fluorophenyl Me Me F H 2,6-dibromo-4-(nonafluoro-n-butylthio)phenyl 1970 2-fluorophenyl Me Me F H 2,6-dichloro-4-(heptafluoroisopropylsulfonyl)phenyl 1971 2-fluorophenyl Me Me F H 2,6-dibromo-4-(heptafluoro-n-propylsulfonyl)phenyl 1972 2-fluorophenyl Me Me F H 2-bromo-6-(heptafluoroisopropyloxy)-4-methylpyridin-3-yl 1973 2-fluorophenyl Me Me F H 2,4-dimethyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1974 2-fluorophenyl Me Me F H 2-chloro-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1975 2-fluorophenyl Me Me F H 2-bromo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl 1976 2-fluorophenyl Me Me F H 2-iodo-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl

TABLE 4

(X, R₂ = a hydrogen atom, A₃, A₄ = a carbon atom, G₁, G₂ = an oxygen atom, n = 0) Comp. No. Q₁ R₁ A₁ A₂ Q₂ 2001 phenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2002 2-methylphenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2003 4-methylphenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2004 2-fluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2005 3-fluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2006 4-fluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2007 2-chlorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2008 4-chlorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2009 2-bromophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2010 2-iodophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2011 3-cyanophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2012 4-cyanophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2013 2-nitrophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2014 3-nitrophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2015 4-nitrophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2016 2-trifluoromethylphenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2017 4-trifluoromethylphenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2018 4-trifluoromethoxyphenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2019 2,3-difluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2020 2,4-difluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2021 2,5-difluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2022 2,6-difluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2023 2,4-dichlorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2024 2,6-dichlorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2025 3,4-dichlorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2026 2-chloro-4-nitrophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2027 2-chloro-4-fluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2028 2-chloro-6-fluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2029 4-chloro-2-fluorophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2030 4-chloro-2-nitrophenyl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2031 2,3,6-trifluoro H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2032 pyridin-2-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2033 pyridin-3-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2034 pyridin-4-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2035 2-fluoropyridin-3-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2036 2-chloropyridin-3-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2037 2-chloropyridin-5-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2038 2-methylthiopyridin-3-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2039 pyrazin-2-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2040 furan-2-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2041 thiophen-2-yl H N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2042 phenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2043 2-methylphenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2044 4-methylphenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2045 2-fluorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2046 3-fluorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2047 4-fluorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2048 2-chlorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2049 4-chlorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2050 2-bromophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2051 2-iodophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2052 3-cyanophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2053 4-cyanophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2054 2-nitrophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2055 3-nitrophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2056 4-nitrophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2057 2-trifluoromethyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2058 4-trifluoromethyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2059 4-trifluoromethoxy H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2060 2,3-difluorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2061 2,4-difluorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2062 2,5-difluorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2063 2,6-difluorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2064 2,4-dichlorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2065 2,6-dichlorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2066 3,4-dichlorophenyl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2067 2-chloro-4-nitro H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2068 2-chloro-4-fluoro H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2069 2-chloro-6-fluoro H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2070 4-chloro-2-fluoro H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2071 4-chloro-2-nitro H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2072 2,3,6-trifluoro H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2073 pyridin-2-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2074 pyridin-3-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2075 2-fluoropyridin-3-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2076 2-chloropyridin-3-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2077 2-chloropyridin-5-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2078 2-methylthiopyridin-3-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2079 pyrazin-2-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2080 furan-2-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2081 thiophen-2-yl H N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2082 phenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2083 2-methylphenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2084 4-methylphenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2085 2-fluorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2086 3-fluorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2087 4-fluorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2088 2-chlorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2089 4-chlorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2090 2-bromophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2091 2-iodophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2092 3-cyanophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2093 4-cyanophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2094 2-nitrophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2095 3-nitrophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2096 4-nitrophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2097 2-trifluoromethyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2098 4-trifluoromethyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2099 4-trifluoromethoxy Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2100 2,3-difluorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2101 2,4-difluorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2102 2,5-difluorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2103 2,6-difluorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2104 2,4-dichlorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2105 2,6-dichlorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2106 3,4-dichlorophenyl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2107 2-chloro-4-nitro Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2108 2-chloro-4-fluoro Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2109 2-chloro-6-fluoro Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2110 4-chloro-2-fluoro Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2111 4-chloro-2-nitro Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2112 2,3,6-trifluoro Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl phenyl 2113 pyridin-2-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2114 pyridin-3-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2115 2-fluoropyridin-3-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2116 2-chloropyridin-3-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2117 2-chloropyridin-5-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2118 2-methylthiopyridin-3-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2119 pyrazin-2-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2120 furan-2-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2121 thiophen-2-yl Me N C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2122 phenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2123 2-methylphenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2124 4-methylphenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2125 2-fluorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2126 3-fluorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2127 4-fluorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2128 2-chlorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2129 4-chlorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2130 2-bromophenyl He N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2131 2-iodophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2132 3-cyanophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2133 4-cyanophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2134 2-nitrophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2135 3-nitrophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2136 4-nitrophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2137 2-trifluoromethyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2138 4-trifluoromethyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2139 4-trifluoromethoxy Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2140 2,3-difluorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2141 2,4-difluorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2142 2,5-difluorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2143 2,6-difluorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2144 2,4-dichlorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2145 2,6-dichlorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2146 3,4-dichlorophenyl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2147 2-chloro-4-nitro Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2148 2-chloro-4-fluoro Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2149 2-chloro-6-fluoro Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2150 4-chloro-2-fluoro Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2151 4-chloro-2-nitro Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2152 2,3,6-trifluoro Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl phenyl 2153 pyridin-2-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2154 pyridin-3-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2155 2-fluoropyridin-3-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2156 2-chloropyridin-3-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2157 2-chloropyridin-5-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2158 2-methylthiopyridin-3-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2159 pyrazin-2-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2160 furan-2-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2161 thiophen-2-yl Me N C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2162 phenyl H C N 2,6-dimethyl-4-heptafluoroisopropylphenyl 2163 phenyl H C N-oxide 2,6-dimethyl-4-heptafluoroisopropylphenyl 2164 phenyl H N-oxide C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2165 2-fluorophenyl H N-oxide C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2166 phenyl H N-oxide C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2167 2-fluorophenyl H N-oxide C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2168 phenyl Me N-oxide C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2169 2-fluorophenyl Me N-oxide C 2,6-dimethyl-4-heptafluoroisopropylphenyl 2170 phenyl Me N-oxide C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2171 2-fluorophenyl Me N-oxide C 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl

TABLE 5

(X₁, X₂, X₃, X₄, R₁, R₂ = a hydrogen atom, Q₁ = phenyl) Comp. No. G₁ G₂ Q₂ 2201 O S 2,6-dimethyl-4-heptafluoroisopropylphenyl 2202 S O 2,6-dimethyl-4-heptafluoroisopropylphenyl 2203 S S 2,6-dimethyl-4-heptafluoroisopropylphenyl 2204 O S 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2205 S O 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2206 S S 2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 2207 O S 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 2208 S O 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 2209 S S 2,6-dimethyl-4-(nonafluoro-2-butyl)phenyl 2210 O S 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl) phenyl 2211 S O 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl) phenyl 2212 S S 2-bromo-4-(heptafluoroisopropyl)-6-(methylsulfonyl) phenyl 2213 O S 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 2214 S O 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 2215 S S 2-n-propyl-6-iodo-4-(heptafluoroisopropyl)phenyl 2216 O S 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 2217 S O 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 2218 S S 2,6-dibromo-4-(heptafluoro-n-propylsulfinyl)phenyl 2219 O S 2,6-dichloro-4-(heptafluoro-n-propylthio)phenyl 2220 S O 2,6-dichloro-4-(heptafluoro-n-propylthio)phenyl 2221 S S 2,6-dichloro-4-(heptafluoro-n-propylthio)phenyl

TABLE 6

(A₁, A₂, A₃, A₄ = a carbon atom, X = a hydrogen atom, n = 0, G₂ = an oxygen atom) Comp. No. R₁ R₂ Y₁ Y₂ Y₃ Y₄ Y₅ I-1 H H Me H heptafluoro-n-propyl H Me I-2 H H Me H heptafluoroisopropyl H Me I-3 H H Me Me heptafluoroisopropyl H Cl I-4 H H Me I heptafluoroisopropyl H Cl I-5 H Me Me H heptafluoroisopropyl H Me I-6 H i-Pr Me H heptafluoroisopropyl H Me I-7 H H Et H heptafluoroisopropyl H Me I-8 H H Et H heptafluoroisopropyl H Et I-9 H H Et H heptafluoroisopropyl H I I-10 H H i-Pr H heptafluoroisopropyl H Me I-11 H H MeO H heptafluoroisopropyl H Me I-12 H H Cl H heptafluoroisopropyl H Et I-13 H H Cl Me heptafluoroisopropyl H Me I-14 H H Br H heptafluoroisopropyl H Me I-15 H H Br H heptafluoroisopropyl H Et I-16 H H Br H heptafluoroisopropyl H n-Pr I-17 H H Br H heptafluoroisopropyl H n-Bu I-18 H H Br Me heptafluoroisopropyl H Me I-19 H H I H heptafluoroisopropyl H Me I-20 H H I H heptafluoroisopropyl H n-Pr I-21 H H Me H nonafluoto-n-butyl H Me I-22 H H Me H nonafluoto-2-butyl H Me I-23 H H Br H trifluoromethylthio H Br I-24 H H Br H trifluoromethylsulfonyl H Br I-25 H H Cl H heptafluoroisopropylthio H Cl I-26 H H Br H heptafluoroisopropylthio H Br I-27 H H Cl H heptafluoro-n-propylthio H Cl I-28 H H Br H heptafluoro-n-propylthio H Br I-29 H H Cl H heptafluoroisopropyl- H Cl sulfonyl I-30 H H Br H nonafluoto-n-butylthio H Br I-31 H H Br H pentafluoroethylthio H Br I-32 H H Br H heptafluoro-n-propyl- H Br sulfinyl I-33 Me H Me H heptafluoro-n-propylthio H Me I-34 H Me Br H heptafluoro-n-propylthio H Br I-35 H H Cl H heptafluoroisopropyl H n-Bu I-36 H H I H heptafluoroisopropyl H n-Bu I-37 H H Br H pentafluoroethyl H Br I-38 H H Cl H heptafluoroisopropyl H s-Bu I-39 H H I H heptafluoroisopropyl H s-Bu I-40 H H Br H heptafluoroisopropyl H Br I-41 H H Cl H pentafluoroethyl H Cl I-42 H H Br H heptafluoroisopropyl H MeSO₂ I-43 Me H Br H heptafluoroisopropyl H MeSO₂ I-44 Me Me Br H heptafluoroisopropyl H MeSO₂ I-45 H H Br H heptafluoroisopropyl H MeSO I-46 Me H Br H heptafluoroisopropyl H MeSO I-47 Me Me Br H heptafluoroisopropyl H MeSO I-48 H H Br H heptafluoroisopropyl H MeS I-49 Me H Br H heptafluoroisopropyl H MeS I-50 Me Me Br H heptafluoroisopropyl H MeS I-51 Me Me Me H heptafluoroisopropyl H Me I-52 Me Me Me H nonafluoto-2-butyl H Me I-53 Me H I H heptafluoroisopropyl H n-Pr I-54 Me Me I H heptafluoroisopropyl H n-Pr I-55 Me Me Br H heptafluoro-n-propylthio H Br I-56 Me H Br H heptafluoro-n-propylthio H Br I-57 H H Br H heptafluoro-n-propyl- H Br sulfinyl I-58 Me H Br H heptafluoro-n-propyl- H Br sulfinyl I-59 Me Me Br H heptafluoro-n-propyl- H Br sulfinyl I-60 H H Br H heptafluoro-n-propyl- H Br sulfonyl I-61 Me H Br H heptafluoro-n-propyl- H Br sulfonyl I-62 Me Me Br H heptafluoro-n-propyl- H Br sulfonyl I-63 Me Me Cl H heptafluoro-n-propylthio H Cl I-64 Me H Cl H heptafluoro-n-propylthio H Cl I-65 H H Cl H heptafluoro-n-propyl- H Cl sulfinyl I-66 Me H Cl H heptafluoro-n-propyl- H Cl sulfinyl I-67 Me Me Cl H heptafluoro-n-propyl- H Cl sulfinyl I-68 H H Cl H heptafluoro-n-propyl- H Cl sulfonyl I-69 Me H Cl H heptafluoro-n-propyl- H Cl sulfonyl I-70 Me Me Cl H heptafluoro-n-propyl- H Cl sulfonyl

TABLE 7

(G₂ = an oxygen atom, Y₂, Y₄ = a hydrogen atom) Comp. No. X₁ X₂ X₃ X₄ R₁ R₂ Y₁ Y₃ Y₅ I-81 Me H H H H H Me heptafluoro- Me isopropyl I-82 H Me H H H H Me heptafluoro- Me isopropyl I-83 H H H Me H H Me heptafluoro- Me isopropyl I-84 F H H H H H Me heptafluoro- Me isopropyl I-85 F H H H H H Me heptafluoro- Me isopropylthio I-86 H F H H H H Me heptafluoro- Me isopropyl I-87 H H H F H H Me heptafluoro- Me isopropyl I-88 Cl H H H H H Me heptafluoro- Me isopropyl I-89 H Cl H H H H Me heptafluoro- Me isopropyl I-90 H H H Cl H H Me heptafluoro- Me isopropyl I-91 Br H H H H H Me heptafluoro- Me isopropyl I-92 H H H I H H Me heptafluoro- Me isopropyl I-93 H H CF₃ H H H Me heptafluoro- Me isopropyl I-94 F H H H H Me Me heptafluoro- Me isopropyl I-95 F H H H Me H Me heptafluoro- Me isopropyl I-96 F H H H Me Me Me heptafluoro- Me isopropyl I-97 F H H H H Me Me nonafluoto- Me 2-butyl I-98 F H H H Me H Me nonafluoto- Me 2-butyl I-99 F H H H Me Me Me nonafluoto- Me 2-butyl I-100 F H H H H Me Br heptafluoro-n- Br propylthio I-101 F H H H Me H Br heptafluoro-n- Br propylthio I-102 F H H H Me Me Br heptafluoro-n- Br propylthio I-103 F H H H H Me Br heptafluoro-n- Br propylsulfinyl I-104 F H H H Me H Br heptafluoro-n- Br propylsulfinyl I-105 F H H H Me Me Br heptafluoro-n- Br propylsulfinyl I-106 F H H H H Me n-Pr heptafluoro- I isopropyl I-107 F H H H Me H n-Pr heptafluoro- I isopropyl I-108 F H H H Me Me n-Pr heptafluoro- I isopropyl I-109 F H H H H Me Br heptafluoro- MeSO₂ isopropyl I-110 F H H H Me H Br heptafluoro- MeSO₂ isopropyl I-111 F H H H Me Me Br heptafluoro- MeSO₂ isopropyl I-112 F H H H H Me Br heptafluoro- MeSO isopropyl I-113 F H H H Me H Br heptafluoro- MeSO isopropyl I-114 F H H H Me Me Br heptafluoro- MeSO isopropyl

TABLE 8

(X₂a, X₃a, X₄a, Y₂a, Y₄a = a hydrogen atom, Y₁a, Y₅a = a methyl group, G₂a = an oxygen atom) Comp. No. X₁a R₂a R_(a) R_(b) R_(c) I-121 H H CF₃ F OH I-122 H H CF₃ F Cl I-123 H H CF₃ F Br I-124 H H CF₃ CF₃ OH I-125 H H CF₃ CF₃ Cl I-126 H H CF₃ CF₃ Br I-127 H H CF₃ C₂F₅ OH I-128 H H CF₃ C₂F₅ Cl I-129 H H CF₃ C₂F₅ Br I-130 F H CF₃ F OH I-131 F H CF₃ F Cl I-132 F H CF₃ F Br I-133 F H CF₃ CF₃ OH I-134 F H CF₃ CF₃ Cl I-135 F H CF₃ CF₃ Br I-136 F H CF₃ C₂F₅ OH I-137 F H CF₃ C₂F₅ Cl I-138 F H CF₃ C₂F₅ Br I-139 Cl H CF₃ F OH I-140 Cl H CF₃ F Cl I-141 Cl H CF₃ F Br I-142 Cl H CF₃ CF₃ OH I-143 Cl H CF₃ CF₃ Cl I-144 Cl H CF₃ CF₃ Br I-145 Cl H CF₃ C₂F₅ OH I-146 Cl H CF₃ C₂F₅ Cl I-147 Cl H CF₃ C₂F₅ Br I-148 H Me CF₃ F OH I-149 H Me CF₃ F Cl I-150 H Me CF₃ F Br I-151 H Me CF₃ CF₃ OH I-152 H Me CF₃ CF₃ Cl I-153 H Me CF₃ CF₃ Br I-154 H Me CF₃ C₂F₅ OH I-155 H Me CF₃ C₂F₅ Cl I-156 H Me CF₃ C₂F₅ Br I-157 F Me CF₃ F OH I-158 F Me CF₃ F Cl I-159 F Me CF₃ F Br I-160 F Me CF₃ CF₃ OH I-161 F Me CF₃ CF₃ Cl I-162 F Me CF₃ CF₃ Br I-163 F Me CF₃ C₂F₅ OH I-164 F Me CF₃ C₂F₅ Cl I-165 F Me CF₃ C₂F₅ Br I-166 Cl Me CF₃ F OH I-167 Cl Me CF₃ F Cl I-168 Cl Me CF₃ F Br I-169 Cl Me CF₃ CF₃ OH I-170 Cl Me CF₃ CF₃ Cl I-171 Cl Me CF₃ CF₃ Br I-172 Cl Me CF₃ C₂F₅ OH I-173 Cl Me CF₃ C₂F₅ Cl I-174 Cl Me CF₃ C₂F₅ Br

TABLE 9

(X₂a, X₃a, X₄a, Y₂a, Y₄a = a hydrogen atom, Y₁a, Y₅a = a methyl group, G₂a = an oxygen atom) Comp. No. X₁a R₁a R₂a R_(a) R_(b) R_(c) I-201 H H H CF₃ F OH I-202 H H H CF₃ F Cl I-203 H H H CF₃ F Br I-204 H H H CF₃ CF₃ OH I-205 H H H CF₃ CF₃ Cl I-206 H H H CF₃ CF₃ Br I-207 H H H CF₃ C₂F₅ OH I-208 H H H CF₃ C₂F₅ Cl I-209 H H H CF₃ C₂F₅ Br I-210 F H H CF₃ F OH I-211 F H H CF₃ F Cl I-212 F H H CF₃ F Br I-213 F H H CF₃ CF₃ OH I-214 F H H CF₃ CF₃ Cl I-215 F H H CF₃ CF₃ Br I-216 F H H CF₃ C₂F₅ OH I-217 F H H CF₃ C₂F₅ Cl I-218 F H H CF₃ C₂F₅ Br I-219 Cl H H CF₃ F OH I-220 Cl H H CF₃ F Cl I-221 Cl H H CF₃ F Br I-222 Cl H H CF₃ CF₃ OH I-223 Cl H H CF₃ CF₃ Cl I-224 Cl H H CF₃ CF₃ Br I-225 Cl H H CF₃ C₂F₅ OH I-226 Cl H H CF₃ C₂F₅ Cl I-227 Cl H H CF₃ C₂F₅ Br I-228 H H Me CF₃ F OH I-229 H H Me CF₃ F Cl I-230 H H Me CF₃ F Br I-231 H H Me CF₃ CF₃ OH I-232 H H Me CF₃ CF₃ Cl I-233 H H Me CF₃ CF₃ Br I-234 H H Me CF₃ C₂F₅ OH I-235 H H Me CF₃ C₂F₅ Cl I-236 H H Me CF₃ C₂F₅ Br I-237 F H Me CF₃ F OH I-238 F H Me CF₃ F Cl I-239 F H Me CF₃ F Br I-240 F H Me CF₃ CF₃ OH I-241 F H Me CF₃ CF₃ Cl I-242 F H Me CF₃ CF₃ Br I-243 F H Me CF₃ C₂F₅ OH I-244 F H Me CF₃ C₂F₅ Cl I-245 F H Me CF₃ C₂F₅ Br I-246 Cl H Me CF₃ F OH I-247 Cl H Me CF₃ F Cl I-248 Cl H Me CF₃ F Br I-249 Cl H Me CF₃ CF₃ OH I-250 Cl H Me CF₃ CF₃ Cl I-251 Cl H Me CF₃ CF₃ Br I-252 Cl H Me CF₃ C₂F₅ OH I-253 Cl H Me CF₃ C₂F₅ Cl I-254 Cl H Me CF₃ C₂F₅ Br I-255 H Me H CF₃ F OH I-256 H Me H CF₃ F Cl I-257 H Me H CF₃ F Br I-258 H Me H CF₃ CF₃ OH I-259 H Me H CF₃ CF₃ Cl I-260 H Me H CF₃ CF₃ Br I-261 H Me H CF₃ C₂F₅ OH I-262 H Me H CF₃ C₂F₅ Cl I-263 H Me H CF₃ C₂F₅ Br I-264 F Me H CF₃ F OH I-265 F Me H CF₃ F Cl I-266 F Me H CF₃ F Br I-267 F Me H CF₃ CF₃ OH I-268 F Me H CF₃ CF₃ Cl I-269 F Me H CF₃ CF₃ Br I-270 F Me H CF₃ C₂F₅ OH I-271 F Me H CF₃ C₂F₅ Cl I-272 F Me H CF₃ C₂F₅ Br I-273 Cl Me H CF₃ F OH I-274 Cl Me H CF₃ F Cl I-275 Cl Me H CF₃ F Br I-276 Cl Me H CF₃ CF₃ OH I-277 Cl Me H CF₃ CF₃ Cl I-278 Cl Me H CF₃ CF₃ Br I-279 Cl Me H CF₃ C₂F₅ OH I-280 Cl Me H CF₃ C₂F₅ Cl I-281 Cl Me H CF₃ C₂F₅ Br I-282 H Me Me CF₃ F OH I-283 H Me Me CF₃ F Cl I-284 H Me Me CF₃ F Br I-285 H Me Me CF₃ CF₃ OH I-286 H Me Me CF₃ CF₃ Cl I-287 H Me Me CF₃ CF₃ Br I-288 H Me Me CF₃ C₂F₅ OH I-289 H Me Me CF₃ C₂F₅ Cl I-290 H Me Me CF₃ C₂F₅ Br I-291 F Me Me CF₃ F OH I-292 F Me Me CF₃ F Cl I-293 F Me Me CF₃ F Br I-294 F Me Me CF₃ CF₃ OH I-295 F Me Me CF₃ CF₃ Cl I-296 F Me Me CF₃ CF₃ Br I-297 F Me Me CF₃ C₂F₅ OH I-298 F Me Me CF₃ C₂F₅ Cl I-299 F Me Me CF₃ C₂F₅ Br I-300 Cl Me Me CF₃ F OH I-301 Cl Me Me CF₃ F Cl I-302 Cl Me Me CF₃ F Br I-303 Cl Me Me CF₃ CF₃ OH I-304 Cl Me Me CF₃ CF₃ Cl I-305 Cl Me Me CF₃ CF₃ Br I-306 Cl Me Me CF₃ C₂F₅ OH I-307 Cl Me Me CF₃ C₂F₅ Cl I-308 Cl Me Me CF₃ C₂F₅ Br

TABLE 10

(X₂a, X₃a, X₄a, Y₂a, Y₄a = a hydrogen atom, G₁a, G₂a = an oxygen atom, R_(a) = a trifluoromethyl group) Comp. No. Q₁a X₁a R₁a R₂a Y₁a Y₅a R_(b) R_(c) I-351 phenyl H H H H H CF₃ OH I-352 2-methylphenyl H H H H H CF₃ OH I-353 3-methylphenyl H H H H H CF₃ OH I-354 4-methylphenyl H H H H H CF₃ OH I-355 2,3-dimethylphenyl H H H H H CF₃ OH I-356 2,4,6-trimethylphenyl H H H H H CF₃ OH I-357 4-ethylphenyl H H H H H CF₃ OH I-358 2-fluorophenyl H H H H H CF₃ OH I-359 3-fluorophenyl H H H H H CF₃ OH I-360 4-fluorophenyl H H H H H CF₃ OH I-361 2-chlorophenyl H H H H H CF₃ OH I-362 3-chlorophenyl H H H H H CF₃ OH I-363 4-chlorophenyl H H H H H CF₃ OH I-364 2-bromophenyl H H H H H CF₃ OH I-365 4-bromophenyl H H H H H CF₃ OH I-366 2-iodophenyl H H H H H CF₃ OH I-367 3-iodophenyl H H H H H CF₃ OH I-368 4-iodophenyl H H H H H CF₃ OH I-369 3-cyanophenyl H H H H H CF₃ OH I-370 4-cyanophenyl H H H H H CF₃ OH I-371 2-nitrophenyl H H H H H CF₃ OH I-372 3-nitrophenyl H H H H H CF₃ OH I-373 4-nitrophenyl H H H H H CF₃ OH I-374 2-trifluoromethylphenyl H H H H H CF₃ OH I-375 4-trifluoromethylphenyl H H H H H CF₃ OH I-376 4-trifluoromethoxyphenyl H H H H H CF₃ OH I-377 2,3-difluorophenyl H H H H H CF₃ OH I-378 2,4-difluorophenyl H H H H H CF₃ OH I-379 2,5-difluorophenyl H H H H H CF₃ OH I-380 2,6-difluorophenyl H H H H H CF₃ OH I-381 2,4-dichlorophenyl H H H H H CF₃ OH I-382 2,6-dichlorophenyl H H H H H CF₃ OH I-383 3,4-dichlorophenyl H H H H H CF₃ OH I-384 4-fluoro-3-nitrophenyl H H H H H CF₃ OH I-385 5-fluoro-2-nitrophenyl H H H H H CF₃ OH I-386 2-chloro-4-nitrophenyl H H H H H CF₃ OH I-387 2-chloro-4-fluorophenyl H H H H H CF₃ OH I-388 3-chloro-4-fluorophenyl H H H H H CF₃ OH I-389 2-chloro-6-fluorophenyl H H H H H CF₃ OH I-390 4-chloro-2-fluorophenyl H H H H H CF₃ OH I-391 4-chloro-2-nitrophenyl H H H H H CF₃ OH I-392 2,3,6-trifluorophenyl H H H H H CF₃ OH I-393 2,3,4,5,6-pentafluorophenyl H H H H H CF₃ OH I-394 pyridin-2-yl H H H H H CF₃ OH I-395 pyridin-3-yl H H H H H CF₃ OH I-396 2-fluoropyridin-3-yl H H H H H CF₃ OH I-397 2-chloropyridin-3-yl H H H H H CF₃ OH I-398 4-chloropyridin-3-yl H H H H H CF₃ OH I-399 2-chloropyridin-5-yl H H H H H CF₃ OH I-400 2-methylthiopyridin-3-yl H H H H H CF₃ OH I-401 2,6-dichloropyridin-3-yl H H H H H CF₃ OH I-402 2,6-dichloropyridin-4-yl H H H H H CF₃ OH I-403 pyrazin-2-yl H H H H H CF₃ OH I-404 furan-2-yl H H H H H CF₃ OH I-405 thiophen-2-yl H H H H H CF₃ OH I-406 thiophen-3-yl H H H H H CF₃ OH I-407 4-methoxyphenyl H H H H H CF₃ OH I-408 3,4,5-trimethoxyphenyl H H H H H CF₃ OH I-409 3-methoxyphenyl H H H H H CF₃ OH I-410 2-methoxyphenyl H H H H H CF₃ OH I-411 3,5-dimethoxyphenyl H H H H H CF₃ OH I-412 2,6-dimethoxyphenyl H H H H H CF₃ OH I-413 4-ethoxyphenyl H H H H H CF₃ OH I-414 2-(4-trifluoromethylphenyl)phenyl H H H H H CF₃ OH I-415 1-phenyl-5-trifluoromethylpyrazol-4-yl H H H H H CF₃ OH I-416 5-methylisoxazol-3-yl H H H H H CF₃ OH I-417 4-methyl-1,2,3-thiadiazol-5-yl H H H H H CF₃ OH I-418 pyrrole-2-yl H H H H H CF₃ OH I-419 phenyl H H H H H CF₃ Cl I-420 2-methylphenyl H H H H H CF₃ Cl I-421 4-methylphenyl H H H H H CF₃ Cl I-422 2-fluorophenyl H H H H H CF₃ Cl I-423 3-fluorophenyl H H H H H CF₃ Cl I-424 4-fluorophenyl H H H H H CF₃ Cl I-425 2-chlorophenyl H H H H H CF₃ Cl I-426 4-chlorophenyl H H H H H CF₃ Cl I-427 2-bromophenyl H H H H H CF₃ Cl I-428 2-iodophenyl H H H H H CF₃ Cl I-429 3-cyanophenyl H H H H H CF₃ Cl I-430 4-cyanophenyl H H H H H CF₃ Cl I-431 2-nitrophenyl H H H H H CF₃ Cl I-432 3-nitrophenyl H H H H H CF₃ Cl I-433 4-nitrophenyl H H H H H CF₃ Cl I-434 2-trifluoromethylphenyl H H H H H CF₃ Cl I-435 4-trifluoromethylphenyl H H H H H CF₃ Cl I-436 4-trifluoromethoxyphenyl H H H H H CF₃ Cl I-437 2,3-difluorophenyl H H H H H CF₃ Cl I-438 2,4-difluorophenyl H H H H H CF₃ Cl I-439 2,5-difluorophenyl H H H H H CF₃ Cl I-440 2,6-difluorophenyl H H H H H CF₃ Cl I-441 2,4-dichlorophenyl H H H H H CF₃ Cl I-442 2,6-dichlorophenyl H H H H H CF₃ Cl I-443 3,4-dichlorophenyl H H H H H CF₃ Cl I-444 2-chloro-4-nitrophenyl H H H H H CF₃ Cl I-445 2-chloro-4-fluorophenyl H H H H H CF₃ Cl I-446 2-chloro-6-fluorophenyl H H H H H CF₃ Cl I-447 4-chloro-2-fluorophenyl H H H H H CF₃ Cl I-448 4-chloro-2-nitrophenyl H H H H H CF₃ Cl I-449 2,3,6-trifluorophenyl H H H H H CF₃ Cl I-450 pyridin-2-yl H H H H H CF₃ Cl I-451 pyridin-3-yl H H H H H CF₃ Cl I-452 2-fluoropyridin-3-yl H H H H H CF₃ Cl I-453 2-chloropyridin-3-yl H H H H H CF₃ Cl I-454 2-chloropyridin-5-yl H H H H H CF₃ Cl I-455 2-methylthiopyridin-3-yl H H H H H CF₃ Cl I-456 pyrazin-2-yl H H H H H CF₃ Cl I-457 furan-2-yl H H H H H CF₃ Cl I-458 thiophen-2-yl H H H H H CF₃ Cl I-459 phenyl F H H H H CF₃ OH I-460 2-methylphenyl F H H H H CF₃ OH I-461 4-methylphenyl F H H H H CF₃ OH I-462 2-fluorophenyl F H H H H CF₃ OH I-463 3-fluorophenyl F H H H H CF₃ OH I-464 4-fluorophenyl F H H H H CF₃ OH I-465 2-chlorophenyl F H H H H CF₃ OH I-466 4-chlorophenyl F H H H H CF₃ OH I-467 2-bromophenyl F H H H H CF₃ OH I-468 2-iodophenyl F H H H H CF₃ OH I-469 3-cyanophenyl F H H H H CF₃ OH I-470 4-cyanophenyl F H H H H CF₃ OH I-471 2-nitrophenyl F H H H H CF₃ OH I-472 3-nitrophenyl F H H H H CF₃ OH I-473 4-nitrophenyl F H H H H CF₃ OH I-474 2-trifluoromethylphenyl F H H H H CF₃ OH I-475 4-trifluoromethylphenyl F H H H H CF₃ OH I-476 4-trifluoromethoxyphenyl F H H H H CF₃ OH I-477 2,3-difluorophenyl F H H H H CF₃ OH I-478 2,4-difluorophenyl F H H H H CF₃ OH I-479 2,5-difluorophenyl F H H H H CF₃ OH I-480 2,6-difluorophenyl F H H H H CF₃ OH I-481 2,4-dichlorophenyl F H H H H CF₃ OH I-482 2,6-dichlorophenyl F H H H H CF₃ OH I-483 3,4-dichlorophenyl F H H H H CF₃ OH I-484 2-chloro-4-nitrophenyl F H H H H CF₃ OH I-485 2-chloro-4-fluorophenyl F H H H H CF₃ OH I-486 2-chloro-6-fluorophenyl F H H H H CF₃ OH I-487 4-chloro-2-fluorophenyl F H H H H CF₃ OH I-488 4-chloro-2-nitrophenyl F H H H H CF₃ OH I-489 2,3,6-trifluorophenyl F H H H H CF₃ OH I-490 pyridin-2-yl F H H H H CF₃ OH I-491 pyridin-3-yl F H H H H CF₃ OH I-492 2-fluoropyridin-3-yl F H H H H CF₃ OH I-493 2-chloropyridin-3-yl F H H H H CF₃ OH I-494 2-chloropyridin-5-yl F H H H H CF₃ OH I-495 2-methylthiopyridin-3-yl F H H H H CF₃ OH I-496 pyrazin-2-yl F H H H H CF₃ OH I-497 furan-2-yl F H H H H CF₃ OH I-498 thiophen-2-yl F H H H H CF₃ OH I-499 phenyl F H H H H CF₃ Cl I-500 2-methylphenyl F H H H H CF₃ Cl I-501 4-methylphenyl F H H H H CF₃ Cl I-502 2-fluorophenyl F H H H H CF₃ Cl I-503 3-fluorophenyl F H H H H CF₃ Cl I-504 4-fluorophenyl F H H H H CF₃ Cl I-505 2-chlorophenyl F H H H H CF₃ Cl I-506 4-chlorophenyl F H H H H CF₃ Cl I-507 2-bromophenyl F H H H H CF₃ Cl I-508 2-iodophenyl F H H H H CF₃ Cl I-509 3-cyanophenyl F H H H H CF₃ Cl I-510 4-cyanophenyl F H H H H CF₃ Cl I-511 2-nitrophenyl F H H H H CF₃ Cl I-512 3-nitrophenyl F H H H H CF₃ Cl I-513 4-nitrophenyl F H H H H CF₃ Cl I-514 2-trifluoromethylphenyl F H H H H CF₃ Cl I-515 4-trifluoromethylphenyl F H H H H CF₃ Cl I-516 4-trifluoromethoxyphenyl F H H H H CF₃ Cl I-517 2,3-difluorophenyl F H H H H CF₃ Cl I-518 2,4-difluorophenyl F H H H H CF₃ Cl I-519 2,5-difluorophenyl F H H H H CF₃ Cl I-520 2,6-difluorophenyl F H H H H CF₃ Cl I-521 2,4-dichlorophenyl F H H H H CF₃ Cl I-522 2,6-dichlorophenyl F H H H H CF₃ Cl I-523 3,4-dichlorophenyl F H H H H CF₃ Cl I-524 2-chloro-4-nitrophenyl F H H H H CF₃ Cl I-525 2-chloro-4-fluorophenyl F H H H H CF₃ Cl I-526 2-chloro-6-fluorophenyl F H H H H CF₃ Cl I-527 4-chloro-2-fluorophenyl F H H H H CF₃ Cl I-528 4-chloro-2-nitrophenyl F H H H H CF₃ Cl I-529 2,3,6-trifluorophenyl F H H H H CF₃ Cl I-530 pyridin-2-yl F H H H H CF₃ Cl I-531 pyridin-3-yl F H H H H CF₃ Cl I-532 2-fluoropyridin-3-yl F H H H H CF₃ Cl I-533 2-chloropyridin-3-yl F H H H H CF₃ Cl I-534 2-chloropyridin-5-yl F H H H H CF₃ Cl I-535 2-methylthiopyridin-3-yl F H H H H CF₃ Cl I-536 pyrazin-2-yl F H H H H CF₃ Cl I-537 furan-2-yl F H H H H CF₃ Cl I-538 thiophen-2-yl F H H H H CF₃ Cl I-539 phenyl H Me H H H CF₃ OH I-540 2-methylphenyl H Me H H H CF₃ OH I-541 4-methylphenyl H Me H H H CF₃ OH I-542 2-fluorophenyl H Me H H H CF₃ OH I-543 3-fluorophenyl H Me H H H CF₃ OH I-544 4-fluorophenyl H Me H H H CF₃ OH I-545 2-chlorophenyl H Me H H H CF₃ OH I-546 4-chlorophenyl H Me H H H CF₃ OH I-547 2-bromophenyl H Me H H H CF₃ OH I-548 2-iodophenyl H Me H H H CF₃ OH I-549 3-cyanophenyl H Me H H H CF₃ OH I-550 4-cyanophenyl H Me H H H CF₃ OH I-551 2-nitrophenyl H Me H H H CF₃ OH I-552 3-nitrophenyl H Me H H H CF₃ OH I-553 4-nitrophenyl H Me H H H CF₃ OH I-554 2-trifluoromethylphenyl H Me H H H CF₃ OH I-555 4-trifluoromethylphenyl H Me H H H CF₃ OH I-556 4-trifluoromethoxyphenyl H Me H H H CF₃ OH I-557 2,3-difluorophenyl H Me H H H CF₃ OH I-558 2,4-difluorophenyl H Me H H H CF₃ OH I-559 2,5-difluorophenyl H Me H H H CF₃ OH I-560 2,6-difluorophenyl H Me H H H CF₃ OH I-561 2,4-dichlorophenyl H Me H H H CF₃ OH I-562 2,6-dichlorophenyl H Me H H H CF₃ OH I-563 3,4-dichlorophenyl H Me H H H CF₃ OH I-564 2-chloro-4-nitrophenyl H Me H H H CF₃ OH I-565 2-chloro-4-fluorophenyl H Me H H H CF₃ OH I-566 2-chloro-6-fluorophenyl H Me H H H CF₃ OH I-567 4-chloro-2-fluorophenyl H Me H H H CF₃ OH I-568 4-chloro-2-nitrophenyl H Me H H H CF₃ OH I-569 2,3,6-trifluorophenyl H Me H H H CF₃ OH I-570 pyridin-2-yl H Me H H H CF₃ OH I-571 pyridin-3-yl H Me H H H CF₃ OH I-572 2-fluoropyridin-3-yl H Me H H H CF₃ OH I-573 2-chloropyridin-3-yl H Me H H H CF₃ OH I-574 2-chloropyridin-5-yl H Me H H H CF₃ OH I-575 2-methylthiopyridin-3-yl H Me H H H CF₃ OH I-576 pyrazin-2-yl H Me H H H CF₃ OH I-577 furan-2-yl H Me H H H CF₃ OH I-578 thiophen-2-yl H Me H H H CF₃ OH I-579 phenyl F Me H H H CF₃ Cl I-580 2-methylphenyl F Me H H H CF₃ Cl I-581 4-methylphenyl F Me H H H CF₃ Cl I-582 2-fluorophenyl F Me H H H CF₃ Cl I-583 3-fluorophenyl F Me H H H CF₃ Cl I-584 4-fluorophenyl F Me H H H CF₃ Cl I-585 2-chlorophenyl F Me H H H CF₃ Cl I-586 4-chlorophenyl F Me H H H CF₃ Cl I-587 2-bromophenyl F Me H H H CF₃ Cl I-588 2-iodophenyl F Me H H H CF₃ Cl I-589 3-cyanophenyl F Me H H H CF₃ Cl I-590 4-cyanophenyl F Me H H H CF₃ Cl I-591 2-nitrophenyl F Me H H H CF₃ Cl I-592 3-nitrophenyl F Me H H H CF₃ Cl I-593 4-nitrophenyl F Me H H H CF₃ Cl I-594 2-trifluoromethylphenyl F Me H H H CF₃ Cl I-595 4-trifluoromethylphenyl F Me H H H CF₃ Cl I-596 4-trifluoromethoxyphenyl F Me H H H CF₃ Cl I-597 2,3-difluorophenyl F Me H H H CF₃ Cl I-598 2,4-difluorophenyl F Me H H H CF₃ Cl I-599 2,5-difluorophenyl F Me H H H CF₃ Cl I-600 2,6-difluorophenyl F Me H H H CF₃ Cl I-601 2,4-dichlorophenyl F Me H H H CF₃ Cl I-602 2,6-dichlorophenyl F Me H H H CF₃ Cl I-603 3,4-dichlorophenyl F Me H H H CF₃ Cl I-604 2-chloro-4-nitrophenyl F Me H H H CF₃ Cl I-605 2-chloro-4-fluorophenyl F Me H H H CF₃ Cl I-606 2-chloro-6-fluorophenyl F Me H H H CF₃ Cl I-607 4-chloro-2-fluorophenyl F Me H H H CF₃ Cl I-608 4-chloro-2-nitrophenyl F Me H H H CF₃ Cl I-609 2,3,6-trifluorophenyl F Me H H H CF₃ Cl I-610 pyridin-2-yl F Me H H H CF₃ Cl I-611 pyridin-3-yl F Me H H H CF₃ Cl I-612 2-fluoropyridin-3-yl F Me H H H CF₃ Cl I-613 2-chloropyridin-3-yl F Me H H H CF₃ Cl I-614 2-chloropyridin-5-yl F Me H H H CF₃ Cl I-615 2-methylthiopyridin-3-yl F Me H H H CF₃ Cl I-616 pyrazin-2-yl F Me H H H CF₃ Cl I-617 furan-2-yl F Me H H H CF₃ Cl I-618 thiophen-2-yl F Me H H H CF₃ Cl I-619 phenyl H Me Me H H CF₃ OH I-620 2-methylphenyl H Me Me H H CF₃ OH I-621 4-methylphenyl H Me Me H H CF₃ OH I-622 2-fluorophenyl H Me Me H H CF₃ OH I-623 3-fluorophenyl H Me Me H H CF₃ OH I-624 4-fluorophenyl H Me Me H H CF₃ OH I-625 2-chlorophenyl H Me Me H H CF₃ OH I-626 4-chlorophenyl H Me Me H H CF₃ OH I-627 2-bromophenyl H Me Me H H CF₃ OH I-628 2-iodophenyl H Me Me H H CF₃ OH I-629 3-cyanophenyl H Me Me H H CF₃ OH I-630 4-cyanophenyl H Me Me H H CF₃ OH I-631 2-nitrophenyl H Me Me H H CF₃ OH I-632 3-nitrophenyl H Me Me H H CF₃ OH I-633 4-nitrophenyl H Me Me H H CF₃ OH I-634 2-trifluoromethylphenyl H Me Me H H CF₃ OH I-635 4-trifluoromethylphenyl H Me Me H H CF₃ OH I-636 4-trifluoromethoxyphenyl H Me Me H H CF₃ OH I-637 2,3-difluorophenyl H Me Me H H CF₃ OH I-638 2,4-difluorophenyl H Me Me H H CF₃ OH I-639 2,5-difluorophenyl H Me Me H H CF₃ OH I-640 2,6-difluorophenyl H Me Me H H CF₃ OH I-641 2,4-dichlorophenyl H Me Me H H CF₃ OH I-642 2,6-dichlorophenyl H Me Me H H CF₃ OH I-643 3,4-dichlorophenyl H Me Me H H CF₃ OH I-644 2-chloro-4-nitrophenyl H Me Me H H CF₃ OH I-645 2-chloro-4-fluorophenyl H Me Me H H CF₃ OH I-646 2-chloro-6-fluorophenyl H Me Me H H CF₃ OH I-647 4-chloro-2-fluorophenyl H Me Me H H CF₃ OH I-648 4-chloro-2-nitrophenyl H Me Me H H CF₃ OH I-649 2,3,6-trifluorophenyl H Me Me H H CF₃ OH I-650 pyridin-2-yl H Me Me H H CF₃ OH I-651 pyridin-3-yl H Me Me H H CF₃ OH I-652 2-fluoropyridin-3-yl H Me Me H H CF₃ OH I-653 2-chloropyridin-3-yl H Me Me H H CF₃ OH I-654 2-chloropyridin-5-yl H Me Me H H CF₃ OH I-655 2-methylthiopyridin-3-yl H Me Me H H CF₃ OH I-656 pyrazin-2-yl H Me Me H H CF₃ OH I-657 furan-2-yl H Me Me H H CF₃ OH I-658 thiophen-2-yl H Me Me H H CF₃ OH I-659 phenyl F Me Me H H CF₃ Cl I-660 2-methylphenyl F Me Me H H CF₃ Cl I-661 4-methylphenyl F Me Me H H CF₃ Cl I-662 2-fluorophenyl F Me Me H H CF₃ Cl I-663 3-fluorophenyl F Me Me H H CF₃ Cl I-664 4-fluorophenyl F Me Me H H CF₃ Cl I-665 2-chlorophenyl F Me Me H H CF₃ Cl I-666 4-chlorophenyl F Me Me H H CF₃ Cl I-667 2-bromophenyl F Me Me H H CF₃ Cl I-668 2-iodophenyl F Me Me H H CF₃ Cl I-669 3-cyanophenyl F Me Me H H CF₃ Cl I-670 4-cyanophenyl F Me Me H H CF₃ Cl I-671 2-nitrophenyl F Me Me H H CF₃ Cl I-672 3-nitrophenyl F Me Me H H CF₃ Cl I-673 4-nitrophenyl F Me Me H H CF₃ Cl I-674 2-trifluoromethylphenyl F Me Me H H CF₃ Cl I-675 4-trifluoromethylphenyl F Me Me H H CF₃ Cl I-676 4-trifluoromethoxyphenyl F Me Me H H CF₃ Cl I-677 2,3-difluorophenyl F Me Me H H CF₃ Cl I-678 2,4-difluorophenyl F Me Me H H CF₃ Cl I-679 2,5-difluorophenyl F Me Me H H CF₃ Cl I-680 2,6-difluorophenyl F Me Me H H CF₃ Cl I-681 2,4-dichlorophenyl F Me Me H H CF₃ Cl I-682 2,6-dichlorophenyl F Me Me H H CF₃ Cl I-683 3,4-dichlorophenyl F Me Me H H CF₃ Cl I-684 2-chloro-4-nitrophenyl F Me Me H H CF₃ Cl I-685 2-chloro-4-fluorophenyl F Me Me H H CF₃ Cl I-686 2-chloro-6-fluorophenyl F Me Me H H CF₃ Cl I-687 4-chloro-2-fluorophenyl F Me Me H H CF₃ Cl I-688 4-chloro-2-nitrophenyl F Me Me H H CF₃ Cl I-689 2,3,6-trifluorophenyl F Me Me H H CF₃ Cl I-690 pyridin-2-yl F Me Me H H CF₃ Cl I-691 pyridin-3-yl F Me Me H H CF₃ Cl I-692 2-fluoropyridin-3-yl F Me Me H H CF₃ Cl I-693 2-chloropyridin-3-yl F Me Me H H CF₃ Cl I-694 2-chloropyridin-5-yl F Me Me H H CF₃ Cl I-695 2-methylthiopyridin-3-yl F Me Me H H CF₃ Cl I-696 pyrazin-2-yl F Me Me H H CF₃ Cl I-697 furan-2-yl F Me Me H H CF₃ Cl I-698 thiophen-2-yl F Me Me H H CF₃ Cl I-699 2-fluorophenyl H H H MeSO₂ Br CF₃ OH I-700 2-fluorophenyl H H H MeSO₂ Br CF., Cl I-701 2-fluorophenyl F H H MeSO₂ Br CF₃ OH I-702 2-fluorophenyl F H H MeSO₂ Br CF₃ Cl I-703 2-fluorophenyl H Me H MeSO₂ Br CF₃ OH I-704 2-fluorophenyl H Me H MeSO₂ Br CF₃ Cl I-705 2-fluorophenyl F Me H MeSO₂ Br CF₃ OH I-706 2-fluorophenyl F Me H MeSO₂ Br CF₃ Cl I-707 2-fluorophenyl H Me Me MeSO₂ Br CF₃ OH I-708 2-fluorophenyl H Me Me MeSO₂ Br CF₃ Cl I-709 2-fluorophenyl F Me Me MeSO₂ Br CF₃ OH I-710 2-fluorophenyl F Me Me MeSO₂ Br CF₃ Cl I-711 2-fluorophenyl H H H n-Pr I CF₃ OH I-712 2-fluorophenyl H H H n-Pr I CF₃ Cl I-713 2-fluorophenyl F H H n-Pr I CF₃ OH I-714 2-fluorophenyl F H H n-Pr I CF₃ Cl I-715 2-fluorophenyl H Me H n-Pr I CF₃ OH I-716 2-fluorophenyl H Me H n-Pr I CF₃ Cl I-717 2-fluorophenyl F Me H n-Pr I CF₃ OH I-718 2-fluorophenyl F Me H n-Pr I CF₃ Cl I-719 2-fluorophenyl H Me Me n-Pr I CF₃ OH I-720 2-fluorophenyl H Me Me n-Pr I CF₃ Cl I-721 2-fluorophenyl F Me Me n-Pr I CF₃ OH I-722 2-fluorophenyl F Me Me n-Pr I CF₃ Cl I-723 2-fluorophenyl H H H H H C₂F₅ OH I-724 2-fluorophenyl H H H H H C₂F₅ Cl I-725 2-fluorophenyl F H H H H C₂F₅ OH I-726 2-fluorophenyl F H H H H C₂F₅ Cl I-727 2-fluorophenyl H Me H H H C₂F₅ OH I-728 2-fluorophenyl H Me H H H C₂F₅ Cl I-729 2-fluorophenyl F Me H H H C₂F₅ OH I-730 2-fluorophenyl F Me H H H C₂F₅ Cl I-731 2-fluorophenyl H Me Me H H C₂F₅ OH I-732 2-fluorophenyl H Me Me H H C₂F₅ Cl I-733 2-fluorophenyl F Me Me H H C₂F₅ OH I-734 2-fluorophenyl F Me Me H H C₂F₅ Cl I-35  2-fluorophenyl H H H H H CF₃ Br I-736 2-fluorophenyl H H H H H CF₃ Br I-737 2-fluorophenyl F H H H H CF₃ Br I-738 2-fluorophenyl F H H H H CF₃ Br I-739 2-fluorophenyl H Me H H H CF₃ Br I-740 2-fluorophenyl H Me H H H CF₃ Br I-741 2-fluorophenyl F Me H H H CF₃ Br I-742 2-fluorophenyl F Me H H H CF₃ Br I-743 2-fluorophenyl H Me Me H H CF₃ Br I-744 2-fluorophenyl H Me Me H H CF₃ Br I-745 2-fluorophenyl F Me Me H H CF₃ Br I-746 2-fluorophenyl F Me Me H H CF₃ Br

Hereinbelow, Table 11 and Table 12 represent the properties of the compounds represented by Formulae (1), (6), (8), (11) and (13). The ¹H-NMR chemical shift values represented therein are based on tetramethylsilane as the internal standard substance, if not described otherwise.

TABLE 11 Comp. No. ¹H-NMR (DMSO-d₆, ppm) 1 (CDCl₃) δ 2.36 (6H, s), 7.36 (2H, s), 7.51-7.65 (5H, m), 7.73 (1H, d, J = 7.8 Hz), 7.86 (1H, d, J = 7.8 Hz), 7.89 (2H, d, J = 7.8 Hz), 8.01 (1H, s), 8.33 (1H, s). 2 δ 7.52-7.63 (4H, m), 7.77 (1H, d, J = 7.8 Hz), 7.98-8.09 (5H, m), 8.39 (1H, s), 10.48 (1H, s), 10.59 (1H, s). 3 δ 7.32-7.39 (2H, m), 7.54-7.63 (2H, m), 7.67-7.72 (1H, m), 7.77 (1H, d, J = 7.8 Hz), 7.98 (1H, d, J = 7.8 Hz), 8.03 (2H, s), 8.34 (1H, s), 10.61 (1H, s), 10.65 (1H, s). 4 δ 7.53-7.63 (4H, m), 7.79 (1H, d, J = 8.3 Hz), 7.99-8.02 (2H, m), 8.08 (1H, dd, J = 2.0, 8.3 Hz), 8.17 (2H, s), 8.39 (1H, d, J = 2.0 Hz), 10.50 (1H, s), 10.63 (1H, s). 5 δ 7.33-7.40 (2H, m), 7.54-7.63 (2H, m), 7.68-7.72 (1H, m), 7.79 (1H, d, J = 7.8 Hz), 7.99 (1H, d, J = 7.8 Hz), 8.17 (2H, s), 8.35 (1H, s), 10.65 (1H, s), 10.67 (1H, s). 6 δ 7.52-7.62 (4H, m), 7.75 (1H, d, J = 7.8 Hz), 7.91 (2H, s), 7.97 (2H, d, J = 7.8 Hz), 8.04 (1H, d, J = 7.8 Hz), 8.36 (1H, s), 10.50 (1H, s), 10.61 (1H, s). 7 δ 7.53-7.64 (4H, m), 7.78 (1H, d, J = 7.8 Hz), 7.99-8.01 (2H, m), 8.06 (2H, s), 8.09 (1H, dd, J = 2.0, 7.8 Hz), 8.39 (1H, s), 10.51 (1H, s), 10.63 (1H, s). 8 δ 7.33-7.40 (2H, m), 7.55-7.63 (2H, m), 7.68-7.72 (1H, m), 7.78 (1H, d, J = 7.8 Hz), 7.99 (1H, d, J = 7.8 Hz), 8.05 (2H, s), 8.34 (1H, s), 10.65 (1H, s), 10.69 (1H, s). 9 δ 2.29 (6H, s), 7.47 (2H, s), 7.51-7.62 (4H, m), 7.75 (1H, d, J = 7.8 Hz), 7.97-8.00 (2H, m), 8.03-8.06 (1H, m), 8.36 (1H, s), 10.00 (1H, s), 10.45 (1H, s). 10 δ 2.37 (6H, s), 7.34 (2H, s), 7.46-7.57 (4H, m), 7.75 (1H, d, J = 7.8 Hz), 7.98-8.01 (2H, m), 8.12 (1H, d, J = 7.3 Hz), 8.34 (1H, s), 8.87 (1H, s), 9.66 (1H, s). 11 (CDCl₃) δ 2.35 (6H, s), 2.52 (3H, s), 7.26-7.31 (2H, m), 7.36 (2H, s), 7.37-7.42 (1H, m), 7.49-7.54 (2H, m), 7.68-7.73 (3H, m), 7.79 (1H, d, J = 7.3 Hz), 8.30 (1H, s). 12 δ 2.30 (6H, s), 2.41 (3H, s), 7.42-7.48 (4H, m), 7.54 (1H, d, J = 7.94 Hz), 7.74-7.82 (3H, m), 8.07 (1H, d, J = 7.94 Hz), 8.35 (1H, s), 9.99 (1H, s), 10.43 (1H, s). 13 δ 2.30 (6H, s), 2.40 (3H, s), 7.35 (2H, d, J = 8.3 Hz), 7.45 (2H, s), 7.53 (1H, t, J = 7.8 Hz), 7.74 (1H, d, J = 7.81 Hz), 7.92 (2H, d, J = 8.3 Hz), 8.07 (1H, d, J = 7.8 Hz), 8.36 (1H, s), 9.98 (1H, s), 10.39 (1H, s). 14 δ 1.18 (3H, t, J = 7.6 Hz), 2.30 (6H, s), 2.76 (2H, q, J = 7.6 Hz), 7.30-7.37 (2H, m), 7.42-7.46 (4H, m), 7.52 (1H, t, J = 8.0 Hz), 7.81 (1H, d, J = 8.0 Hz), 7.96 (1H, d, J = 8.0 Hz), 8.35 (1H, s), 9.98 (1H, s), 10.56 (1H, s). 16 δ 1.22 (3H, t, J = 7.6 Hz), 2.31 (6H, s), 2.69 (2H, q, J = 7.6 Hz), 7.39 (2H, d, J = 8.3 Hz), 7.45 (2H, t, J = 7.9 Hz), 7.53 (2H, d, J = 8.3 Hz), 7.74 (1H, d, J = 7.9 Hz), 7.94 (1H, d, J = 8.3 Hz), 8.07 (1H, d, J = 7.9 Hz), 8.36 (1H, s), 9.99 (1H, s), 10.40 (1H, s). 17 δ 2.30 (6H, s), 7.33-7.76 (8H, m), 7.97 (1H, d, J = 8.30 Hz), 8.30 (1H, s), 10.01 (1H, s), 10.65 (1H, s). 18 δ 2.30 (6H, s), 7.45-7.64 (5H, m), 7.76-8.05 (3H, m), 8.06 (1H, d, J = 8.3 Hz), 8.35 (1H, s), 10.00 (1H, s), 10.54 (1H, s). 19 δ 2.30 (6H, s), 7.37-7.45 (4H, m), 7.54 (1H, t, J = 7.8 Hz), 7.76 (1H, d, J = 7.8 Hz), 8.05-8.11 (3H, m), 8.34 (1H, s), 10.00 (1H, s), 10.49 (1H, s). 20 (CDCl₃) δ 2.35 (6H, s), 7.36 (2H, s), 7.37-7.54 (4H, m), 7.69-7.83 (4H, m), 8.13 (1H, s), 8.33 (1H, s). 22 δ 2.30 (6H, s), 7.45 (2H, s), 7.56 (1H, dd, J = 7.8, 6.8 Hz), 7.63 (1H, d, J = 8.8 Hz), 7.72 (1H, d, J = 8.8 Hz), 7.77 (1H, d, J = 6.8 Hz), 7.94 (1H, d, J = 8.3 Hz), 8.03 (1H, d, J = 8.8 Hz), 8.17 (1H, d, J = 7.8 Hz), 8.34 (1H, s), 9.99 (1H, s), 10.54 (1H, s). 23 (CDCl₃) δ 2.36 (6H, s), 7.34-7.38 (3H, m), 7.42-7.46 (1H, m), 7.53 (1H, t, J = 7.8 Hz), 7.62 (1H, s), 7.65-7.68 (2H, m), 7.73-7.75 (1H, m), 7.82-7.84 (1H, m), 7.89 (1H, s), 8.32 (1H, s). 26 (CDCl₃) δ 2.36 (6H, s), 7.19 (1H, dt, J = 2.0, 7.8 Hz), 7.36 (2H, s), 7.46 (1H, t, J = 7.8 Hz), 7.52-7.57 (3H, m), 7.66 (1H, s), 7.74 (1H, d, J = 7.8 Hz), 7.85 (1H, d, J = 7.8 Hz), 7.94 (1H, d, J = 7.8 Hz), 8.31 (1H, s) 28 δ 2.36 (6H, s), 7.33 (2H, s), 7.48 (1H, t, J = 7.8 Hz), 7.75-7.84 (5H, m), 8.14 (1H, d, J = 7.8 Hz), 8.31 (1H, s), 9.20 (1H, s), 10.04 (1H, s). 29 δ 2.30 (6H, s), 7.45 (2H, s), 7.57 (1H, d, J = 7.8 Hz), 7.75-7.80 (2H, m), 8.06-8.11 (2H, m), 8.29 (1H, d, J = 7.8 Hz), 8.34 (1H, s), 8.46 (1H, s), 10.02 (1H, s), 10.65 (1H, s). 30 δ 2.30 (6H, s), 7.45 (2H, s), 7.56 (1H, t, J = 7.8 Hz), 7.79 (1H, d, J = 7.8 Hz), 8.04-8.06 (3H, m), 8.16 (2H, d, J = 8.3 Hz), 8.36 (1H, s), 10.02 (1H, s), 10.72 (1H, s). 31 δ 2.30 (6H, s), 7.45 (2H, s), 7.56 (1H, d, J = 7.8 Hz), 7.76-7.81 (3H, m), 7.88-7.94 (2H, m), 8.17 (1H, d, J = 7.8 Hz), 8.24 (1H, s), 10.02 (1H, s), 10.90 (1H, s). 32 δ 2.32 (6H, s), 7.46 (2H, s), 7.58 (1H, t, J = 7.8 Hz), 7.80-7.89 (2H, m), 8.11 (1H, d, J = 7.8 Hz), 8.36 (1H, s), 8.44-8.48 (2H, m), 8.86 (1H, s), 10.04 (1H, s), 10.83 (1H, s). 33 δ 2.31 (6H, s), 7.45 (2H, s), 7.57 (1H, t, J = 8.1 Hz), 7.80 (1H, d, J = 8.1 Hz), 8.08 (1H, d, J = 8.1 Hz), 8.24 (1H, s), 8.36-8.41 (4H, m), 10.01 (1H, s), 10.79 (1H, s). 34 δ 2.30 (6H, s), 6.39 (2H, s), 6.58-6.62 (1H, m), 6.76 (1H, dd, J = 1.0, 8.3 Hz), 7.19-7.24 (1H, m), 7.45 (2H, s), 7.51 (1H, t, J = 7.8 Hz), 7.66-7.73 (2H, m), 7.94-7.97 (1H, m), 8.30 (1H, d, J = 2.0 Hz), 9.96 (1H, s), 10.20 (1H, s). 35 δ 2.30 (6H, s), 6.53-6.86 (1H, m), 7.20-7.21 (4H, m), 7.45 (2H, s), 7.52 (1H, t, J = 7.8 Hz), 7.73 (1H, d, J = 7.8 Hz), 8.02 (1H, d, J = 7.8 Hz), 8.35 (1H, s), 9.96 (1H, s), 10.32 (1H, s). 37 (CDCl₃) δ 2.34 (6H, s), 7.35 (2H, s), 7.51 (1H, t, J = 7.8 Hz), 7.62- 7.80 (8H, m), 8.25 (1H, s). 39 δ 2.31 (6H, s), 7.45 (2H, s), 7.57 (1H, t, J = 7.8 Hz), 7.79 (1H, d, J = 7.8 Hz), 7.94 (2H, d, J = 8.3 Hz), 8.07 (1H, d, J = 7.8 Hz), 8.20 (2H, d, J = 8.3 Hz), 8.36 (1H, s), 10.01 (1H, s), 10.70 (1H, s). 40 δ 2.30 (6H, s), 6.96-7.01 (2H, m), 7.43-7.48 (3H, m), 7.56 (1H, t, J = 8.3 Hz), 7.78 (1H, d, J = 8.3 Hz), 7.97-8.00 (2H, m), 8.29 (1H, s), 10.01 (1H, s), 10.61 (1H, s). 41 δ 2.30 (6H, s), 3.90 (3H, s), 7.05-7.10 (1H, m), 7.19 (1H, d, J = 8.3 Hz), 7.45 (2H, s), 7.49-7.54 (2H, m), 7.63 (1H, dd, J = 2.0, 7.8 Hz), 7.72 (1H, d, J = 7.8 Hz), 7.96 (1H, d, J = 7.8 Hz), 8.33 (1H, s), 9.98 (1H, s), 10.33 (1H, s). 45 δ 1.33 (9H, s), 2.31 (6H, s), 7.45 (2H, s), 7.53 (1H, t, J = 7.8 Hz), 7.54 (2H, d, J = 8.3 Hz), 7.74 (1H, d, J = 7.8 Hz), 7.94 (2H, d, J = 8.3 Hz), 8.06 (1H, d, J = 7.8 Hz), 8.36 (1H, s), 9.99 (1H, s), 10.40 (1H, s). 46 δ 2.30 (6H, s), 2.98 (6H, s), 6.93-6.95 (1H, m), 7.25-7.35 (3H, m), 7.45 (2H, s), 7.53 (1H, t, J = 7.8 Hz), 7.74 (1H, d, J = 7.8 Hz), 8.06 (1H, d, J = 7.8 Hz), 8.35 (1H, s), 9.99 (1H, s), 10.35 (1H, s). 47 δ 2.30 (6H, s), 3.01 (6H, s), 6.77 (2H, d, J = 9.3 Hz), 7.45 (2H, s), 7.50 (1H, t, J = 7.8 Hz), 7.69 (1H, d, J = 7.8 Hz), 7.91 (2H, d, J = 9.3 Hz), 8.06 (1H, d, J = 7.8 Hz), 8.33 (1H, s), 9.96 (1H, s), 10.09 (1H, s). 48 δ 2.31 (6H, s), 7.45 (2H, s), 7.53-7.60 (3H, m), 7.77 (1H, d, J = 7.3 Hz), 8.06 (1H, d, J = 8.3 Hz), 8.13 (2H, d, J = 8.3 Hz), 8.35 (1H, s), 10.01 (1H, s), 10.59 (1H, s). 52 δ 2.21 (3H, s), 2.30 (6H, s), 7.27 (1H, d, J = 8.3 Hz), 7.39-7.44 (1H, m), 7.45 (2H, s), 7.50-7.62 (2H, m), 7.70-7.52 (2H, m), 7.92 (1H, d, J = 7.8 Hz), 8.29 (1H, s), 9.99 (1H, s), 10.57 (1H, s). 54 δ 2.30 (6H, s), 3.91 (3H, s), 7.45 (2H, s), 7.56 (1H, t, J = 7.8 Hz), 7.78 (1H, d, J = 7.8 Hz), 8.03-8.15 (5H, m), 8.36 (1H, s), 10.01 (1H, s), 10.67 (1H, s). 56 δ 2.27 (6H, s), 2.30 (6H, s), 7.18-7.22 (1H, m), 7.26-7.30 (2H, m), 7.45 (2H, s), 7.52 (1H, t, J = 7.8 Hz), 7.72 (1H, d, J = 7.8 Hz), 7.95 (1H, d, J = 7.8 Hz), 8.36 (1H, s), 9.98 (1H, s), 10.52 (1H, s). 57 δ 2.30 (6H, s), 2.33 (3H, s), 2.38 (3H, s), 7.11-7.13 (2H, m), 7.40 (1H, d, J = 7.8 Hz), 7.44 (2H, s), 7.51 (1H, t, J = 7.8 Hz), 7.72 (1H, d, J = 7.8 Hz), 7.95 (1H, d, J = 8.8 Hz), 8.34 (1H, s), 9.98 (1H, s), 10.43 (1H, s). 58 δ 2.30 (12H, s), 7.12 (2H, d, J = 7.8 Hz), 7.23-7.27 (1H, m), 7.45 (2H, s), 7.52 (1H, t, J = 8.3 Hz), 7.75 (1H, d, J = 8.3 Hz), 7.94-7.99 (1H, m), 8.35 (1H, s), 10.00 (1H, s), 10.61 (1H, s). 59 δ 2.30 (6H, s), 7.34-7.40 (1H, m), 7.45 (2H, s), 7.50-7.58 (2H, m), 7.60-7.68 (1H, m), 7.77 (1H, d, J = 7.8 Hz), 7.96 (1H, d, J = 8.3 Hz), 8.31 (1H, s), 10.02 (1H, s), 10.78 (1H, s). 60 δ 2.30 (6H, s), 7.22-7.28 (1H, m), 7.42-7.48 (3H, m), 7.53-7.57 (1H, m), 7.75-7.82 (2H, m), 7.96 (1H, d, J = 7.8 Hz), 8.30 (1H, s), 10.01 (1H, s), 10.65 (1H, s). 61 δ 2.30 (6H, s), 7.45 (2H, s), 7.46-7.49 (2H, m), 7.53-7.59 (2H, m), 7.77 (1H, d, J = 7.8 Hz), 7.96 (1H, d, J = 8.3 Hz), 8.30 (1H, s), 10.02 (1H, broad), 10.72 (1H, broad). 62 δ 2.30 (6H, s), 7.25-7.30 (2H, m), 7.45 (2H, s), 7.54-7.65 (2H, m), 7.77 (1H, d, J = 7.8 Hz), 7.93 (1H, d, J = 7.8 Hz), 8.29 (1H, s), 10.03 (1H, s), 11.04 (1H, s). 66 δ 2.30 (6H, s), 7.45 (2H, s), 7.52-7.62 (2H, m), 7.66 (1H, d, J = 8.3 Hz), 7.75-7.80 (2H, m), 7.94 (1H, d, J = 7.8 Hz), 8.30 (1H, s), 10.02 (1H, s), 10.77 (1H, s). 68 δ 2.30 (6H, s), 7.45 (2H, s), 7.50-7.62 (4H, m), 7.78 (1H, d, J = 7.8 Hz), 7.94 (1H, d, J = 7.8 Hz), 8.28 (1H, s), 10.03 (1H, s), 10.99 (1H, s). 69 δ 2.30 (6H, s), 7.45 (2H, s), 7.56 (1H, t, J = 7.8 Hz), 7.79 (1H, d, J = 7.8 Hz), 7.85 (1H, d, J = 8.3 Hz), 7.97-8.00 (1H, m), 8.05-8.08 (1H, m), 8.27 (1H, d, J = 2.0 Hz), 8.33 (1H, s), 10.00 (1H, s), 10.61 (1H, s). 70 δ 2.74 (6H, s), 7.34 (2H, s), 7.52 (1H, t, J = 7.8 Hz), 7.81 (1H, d, J = 7.8 Hz), 7.93 (1H, d, J = 8.3 Hz), 8.13-8.15 (2H, m), 8.58 (1H, d, J = 8.3 Hz), 8.94 (1H, s), 9.27 (1H, s), 10.67 (1H, s). 71 (CDCl₃) δ 1.6-2.4 (6H, broad-s), 6.5-7.7 (3H, broad), 7.8-8.0 (4H, broad), 8.10 (1H, broad-s), 8.28 (1H, d, J = 8.8 Hz). 72 δ 2.30 (6H, s), 3.78 (6H, s), 6.66-6.75 (2H, m), 7.34-7.50 (4H, m), 7.67 (1H, d, J = 7.8 Hz), 7.91 (1H, d, J = 7.8 Hz), 8.34 (1H, s), 9.98 (1H, s), 10.44 (1H, s). 73 δ 2.30 (6H, s), 3.83 (6H, s), 6.73 (1H, t, J = 2.4 Hz), 7.15 (2H, d, J = 2.4 Hz), 7.45 (2H, s), 7.54 (1H, t, J = 8.3 Hz), 7.75 (1H, d, J = 8.3 Hz), 8.06 (1H, d, J = 8.3 Hz), 8.33 (1H, s), 9.99 (1H, s), 10.39 (1H, s). 74 (CDCl₃) δ 2.34 (6H, s), 2.68 (3H, s), 7.36 (2H, s), 7.55 (1H, t, J = 7.8 Hz), 7.62 (1H, s), 7.72 (1H, d, J = 7.8 Hz), 7.81 (1H, d, J = 8.3 Hz), 7.88 (1H, s), 7.92 (1H, d, J = 7.8 Hz), 8.05 (1H, d, J = 8.3 Hz), 8.17 (1H, s), 8.26 (1H, s). 75 δ 2.30 (6H, s), 5.22 (2H, broad-s), 6.67-6.72 (1H, m), 6.78-6.81 (1H, m), 6.97-7.02 (1H, m), 7.45 (2H, s), 7.52 (1H, t, J = 7.8 Hz), 7.72 (1H, d, J = 7.8 Hz), 7.94 (1H, d, J = 7.8 Hz), 8.32 (1H, s), 9.98 (1H, s), 10.46 (1H, s). 77 δ 2.30 (6H, s), 7.45 (2H, s), 7.58 (1H, t, J = 7.8 Hz), 7.70 (1H, t, J = 8.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.99 (1H, d, J = 7.8 Hz), 8.29 (1H, s), 8.45-8.50 (1H, m), 8.57-8.60 (1H, m), 10.03 (1H, s), 10.91 (1H, s). 81 δ 2.30 (6H, s), 7.56 (1H, t), 7.73-7.80 (6H, m), 7.92 (1H, d, J = 7.81 Hz), 8.22 (1H, s), 10.03 (1H, s), 11.05 (1H, s). 82 δ 2.30 (6H, s), 7.45 (2H, s), 7.57 (1H, t, J = 7.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.92-7.96 (2H, m), 8.29-8.45 (2H, m), 8.45 (1H, m), 10.03 (1H, s), 10.98 (1H, s). 83 δ 2.28 (6H, s), 7.33-7.38 (1H, m), 7.43 (2H, s), 7.53 (1H, t, J = 7.9 Hz), 7.58 (1H, d, J = 2.4 Hz), 7.61-7.71 (1H, m), 7.75 (1H, d, J = 7.9 Hz), 7.93 (1H, d, J = 7.9 Hz), 8.28 (1H, s), 9.98 (1H, s), 10.71 (1H, s). 84 δ 2.30 (6H, s), 7.38-7.48 (4H, m), 7.54-7.60 (2H, m), 7.78 (1H, d, J = 7.8 Hz), 7.93 (1H, d, J = 7.8 Hz), 8.28 (1H, s), 10.03 (1H, s), 11.03 (1H, s). 86 δ 2.30 (6H, s), 7.42-7.47 (3H, m), 7.55 (1H, t, J = 8.0 Hz), 7.64 (1H, d, J = 2.0 Hz), 7.66-7.77 (2H, m), 7.96 (1H, d, J = 8.0 Hz), 8.29 (1H, s), 10.01 (1H, s), 10.69 (1H, s). 87 δ 2.30 (6H, s), 7.45 (2H, s), 7.56 (1H, t, J = 7.9 Hz), 7.79 (1H, d, J = 7.9 Hz), 7.87 (1H, d, J = 7.9 Hz), 7.92 (1H, dd, J = 8.2, 1.6 Hz), 8.00 (1H, dd, J = 8.2, 1.6 Hz), 8.22 (1H, t, J = 1.6 Hz), 8.29 (1H, d, J = 1.6 Hz), 10.03 (1H, s), 10.94 (1H, s). 88 (CDCl₃) δ 2.37 (6H, s), 4.06 (3H, s), 7.37 (2H, s), 7.44 (1H, d, J = 9.7 Hz), 7.52 (1H, s), 7.58 (1H, t, J = 7.8 Hz), 7.70 (1H, s), 7.74 (1H, d, J = 7.8 Hz), 7.93 (1H, s), 7.95 (1H, s), 8.02 (1H, s), 8.26 (1H, s). 89 (CDCl₃) δ 2.37 (6H, s), 4.22 (3H, s), 7.37 (2H, s), 7.55 (1H, t, J = 7.8 Hz), 7.56 (1H, s), 7.72 (1H, d, J = 7.8 Hz), 7.94-7.97 (2H, m), 8.00 (1H, d, J = 7.8 Hz), 8.28 (1H, s), 8.47 (1H, d, J = 8.8 Hz), 9.83 (1H, s). 91 δ 2.25 (6H, s), 2.27 (3H, s), 2.29 (6H, s), 6.94 (2H, s), 7.45 (2H, s), 7.51 (1H, t, J = 7.8 Hz), 7.73 (1H, d, J = 7.8 Hz), 7.94 (1H, d, J = 7.8 Hz), 8.34 (1H, s), 9.97 (1H, s), 10.53 (1H, s). 92 δ 2.33 (6H, s), 7.32-7.40 (1H, m), 7.45 (2H, s), 7.58 (1H, t, J = 8.06 Hz), 7.67-7.75 (1H, m), 7.80 (1H, d, J = 7.81 Hz), 7.92 (1H, d, J = 8.29 Hz), 8.27 (1H, s), 10.04 (1H, s), 11.14 (1H, s). 95 δ 2.30 (6H, s), 7.45 (2H, s), 7.59 (1H, t, J = 7.8 Hz), 7.83 (1H, d, J = 7.8 Hz), 7.91-7.94 (1H, dd, J = 1.5, 7.8 Hz), 8.25 (1H, d, J = 1.5 Hz), 10.06 (1H, s), 11.27 (1H, s). 96 δ 2.30 (6H, s), 7.28-7.55 (10H, m), 7.57-7.61 (2H, m), 7.69 (1H, d, J = 7.8 Hz), 7.74 (1H, d, J = 7.8 Hz), 8.13 (1H, s), 9.94 (1H, s), 10.47 (1H, s). 97 δ 2.32 (6H, s), 7.41-7.57 (6H, m), 7.72-7.82 (3H, m), 7.85-7.88 (2H, m), 8.09-8.13 (3H, m), 8.40 (1H, s), 10.01 (1H, s), 10.53 (1H, s). 98 δ 2.31 (6H, s), 7.45 (2H, s), 7.54-7.65 (4H, m), 7.76-7.80 (2H, m), 8.01-8.06 (2H, m), 8.10 (1H, d, J = 8.3 Hz), 8.21-8.23 (1H, m), 8.43 (1H, s), 10.01 (1H, s), 10.80 (1H, s). 99 δ 2.32 (6H, s), 7.46 (2H, s), 7.57 (1H, t, J = 7.8 Hz), 7.61-7.72 (2H, m), 7.78 (1H, d, J = 7.8 Hz), 7.99-8.17 (5H, m), 8.41 (1H, t, J = 2.0 Hz), 8.65 (1H, s), 10.01 (1H, s), 10.66 (1H, s). 100 δ 2.31 (6H, s), 7.45 (2H, s), 7.55 (1H, t, J = 7.8 Hz), 7.69-7.76 (2H, m), 8.07-8.14 (2H, m), 8.19 (1H, d, J = 7.8 Hz), 8.54 (1H, s), 8.77 (1H, d, J = 4.9 Hz), 9.99 (1H, s), 10.86 (1H, s). 101 δ 2.30 (6H, s), 7.45 (2H, s), 7.54-7.61 (2H, m), 7.78 (1H, d, J = 8.3 Hz), 8.06 (1H, d, J = 7.3 Hz), 8.32-8.35 (2H, m), 8.77-8.79 (1H, m), 9.14 (1H, d, J = 1.5 Hz), 10.00 (1H, s), 10.66 (1H, s). 102 δ 2.30 (6H, s), 7.45 (2H, s), 7.57 (1H, t, J = 7.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.91 (2H, d, J = 5.6 Hz), 8.06 (1H, d, J = 7.8 Hz), 8.35 (1H, s), 8.81 (2H, d, J = 5.6 Hz), 10.01 (1H, s), 10.72 (1H, s). 103 δ 2.27 (3H, s), 2.30 (6H, s), 7.45 (2H, s), 7.54-8.07 (6H, m), 8.35 (1H, s), 10.02 (1H, s), 10.77 (1H, s). 105 δ 2.30 (6H, s), 7.45 (2H, s), 7.52-7.58 (2H, m), 7.78 (1H, d, J = 8.30 Hz), 7.97 (1H, d, J = 8.29 Hz), 8.26-8.31 (2H, m), 8.42 (1H, d, J = 4.39 Hz), 10.02 (1H, s), 10.80 (1H, s). 106 δ 2.30 (6H, s), 7.45 (2H, s), 7.54-7.60 (2H, m), 7.77-7.81 (1H, m), 7.95 (1H, d, J = 7.8 Hz), 8.10-8.13 (1H, m), 8.30 (1H, s), 8.54-8.59 (1H, m), 10.03 (1H, s), 10.88 (1H, s). 108 δ 2.31 (6H, s), 7.45 (2H, s), 7.56 (1H, t, J = 7.8 Hz), 7.78 (1H, d, J = 7.8 Hz), 7.82 (1H, dd, J = 6.3, 2.4 Hz), 8.11-8.16 (3H, m), 8.47 (1H, s), 10.01 (1H, s), 10.69 (1H, s). 109 δ 2.31 (6H, s), 7.46 (2H, s), 7.57 (1H, t, J = 8.3 Hz), 7.74 (1H, d, J = 8.3 Hz), 7.80 (1H, d, J = 8.3 Hz), 8.06 (1H, dd, J = 8.3, 1.7 Hz), 8.34 (1H, t, J = 1.7 Hz), 8.40 (1H, dd, J = 8.3, 1.7 Hz), 9.00 (1H, d, J = 1.7 Hz), 10.02 (1H, s), 10.71 (1H, s). 110 δ 2.31 (6H, s), 7.45 (2H, s), 7.56 (1H, d, J = 8.1 Hz), 7.78 (1H, d, J = 8.1 Hz), 7.86 (1H, d, J = 2.1 Hz), 8.11 (1H, dd, J = 8.1, 2.1 Hz), 8.19 (1H, d, J = 2.1 Hz), 8.53 (1H, t, J = 2.1 Hz), 8.75 (1H, d, J = 5.4 Hz), 10.01 (1H, s), 10.96 (1H, s). 111 (CDCl₃) δ 2.36 (6H, s,), 7.34 (2H, s,), 7.47-8.94 (7H, m,), 9.63 (1H, s,), 10.73 (1H, s,). 113 (CDCl₃) δ 2.36 (6H, s,), 7.34-8.73 (15H, m, Ar,), 10.01 (1H, s,) 114 δ 2.30 (6H, s), 2.42 (3H, s), 7.25-7.28 (1H, m), 7.44 (2H, s), 7.55 (1H, t, J = 7.8 Hz), 7.77 (1H, d, J = 7.8 Hz), 7.94-7.97 (2H, m), 8.30 (1H, s), 8.61 (1H, dd, J = 4.9, 1.5 Hz), 10.00 (1H, s), 10.67 (1H, s). 115 δ 2.29 (6H, s), 3.94 (3H, s), 4.06 (3H, s), 6.53 (1H, d, J = 8.3 Hz), 7.44 (2H, s), 7.51 (1H, t, J = 7.9 Hz), 7.72 (1H, d, J = 7.9 Hz), 7.95 (1H, d, J = 7.9 Hz), 8.12 (1H, d, J = 8.3 Hz), 8.28 (1H, s), 9.96 (1H, s), 10.07 (1H, s). 116 δ 2.29 (6H, s), 7.44 (2H, s), 7.57 (1H, t, J = 7.9 Hz), 7.80 (1H, d, J = 7.9 Hz), 8.05 (1H, d, J = 7.9 Hz), 8.30 (1H, s), 8.67 (1H, d, J = 2.2 Hz), 8.93 (1H, d, J = 2.2 Hz), 10.01 (1H, s), 10.73 (1H, s). 117 (CDCl₃) δ 2.36 (6H, s), 7.37-8.50 (9H, m,), 8.97 (1H, s). 118 δ 2.28 (6H, s), 7.43 (2H, s), 7.56 (1H, t, J = 8.0 Hz), 7.74-7.79 (2H, m), 7.92 (1H, d, J = 8.0 Hz), 8.20 (1H, d, J = 8.3 Hz), 8.25 (1H, s), 10.01 (1H, s), 10.88 (1H, s). 119 (CDCl₃) δ 2.36 (6H, s), 7.36-8.60 (10H, m,). 120 δ 2.31 (6H, s), 7.46 (2H, s), 7.57 (1H, t, J = 7.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 8.02 (1H, d, J = 7.8 Hz), 8.08 (2H, d, J = 1.2 Hz), 8.33 (1H, t, J = 2.0 Hz), 8.40 (2H, d, J = 7.3 Hz), 10.02 (1H, s), 10.63 (1H, s). 121 δ 2.30 (6H, s), 3.89 (3H, s), 6.11 (1H, dd, J = 2.0, 3.9 Hz), 7.03 (1H, t, J = 2.0 Hz), 7.10 (1H, dd, J = 2.0, 3.9 Hz), 7.45 (2H, s), 7.49 (1H, t, J = 7.8 Hz), 7.69 (1H, d, J = 7.8 Hz), 7.99 (1H, d, J = 7.8 Hz), 8.28 (1H, s), 9.95 (2H, s). 122 δ 2.31 (6H, s), 7.45 (2H, s), 7.57 (1H, t, J = 7.8 Hz), 7.78 (1H, d, J = 7.8 Hz), 8.11 (1H, d, J = 7.8 Hz), 8.53 (1H, s), 8.84 (1H, dd, J = 1.5, 2.4 Hz), 8.95 (1H, d, J = 2.4 Hz), 9.33 (1H, d, J = 1.5 Hz), 10.00 (1H, s), 10.97 (1H, s). 124 δ 2.28 (6H, s), 7.44 (2H, s), 7.58 (1H, t, J = 7.9 Hz), 7.81 (1H, d, J = 7.9 Hz), 7.92 (1H, d, J = 7.9 Hz), 8.20 (1H, s), 9.43 (1H, s), 9.59 (1H, s), 10.03 (1H, s), 11.06 (1H, s). 125 δ 2.30 (6H, s), 7.45 (2H, s), 7.50-7.62 (4H, m), 7.78 (1H, d, J = 7.8 Hz), 7.94 (1H, d, J = 7.8 Hz), 8.28 (1H, s), 10.03 (1H, s), 10.99 (1H, s). 126 δ 2.30 (6H, s), 7.04 (1H, t, J = 1.5 Hz), 7.45 (2H, s), 7.53 (1H, t, J = 8.0 Hz), 7.74-7.82 (2H, m), 8.04 (1H, d, J = 1.5 Hz), 8.25 (1H, d, J = 1.5 Hz), 8.43 (1H, t, J = 1.5 Hz), 9.98 (1H, s), 10.14 (1H, s). 127 δ 1.86-1.91 (2H, m), 2.00-2.02 (1H, m), 2.19-2.29 (7H, m), 3.81- 3.87 (1H, m), 3.98-4.03 (1H, m), 4.40-4.43 (1H, m), 7.44-7.50 (3H, m), 7.77 (1H, d, J = 7.8 Hz), 7.94 (1H, d, J = 7.8 Hz), 8.26 (1H, s), 9.89 (1H, s), 9.94 (1H, s). 128 (CDCl₃) δ 2.02-2.10 (2H, m), 2.28 (6H, s), 3.15-3.22 (1H, m), 3.80- 3.98 (4H, m), 7.44 (2H, s), 7.48 (1H, t, J = 7.8 Hz), 7.68 (1H, t, J = 7.8 Hz), 7.87 (1H, d, J = 7.8 Hz), 8.16 (1H, s), 9.96 (1H, s), 10.3 (1H, s). 129 (CDCl₃) δ 2.22 (6H, s), 7.17-7.28 (3H, m), 7.33-7.39 (2H, m), 7.42- .48 (2H, m), 7.58-7.65 (2H, m), 7.79 (1H, dd, J = 1.5, 8.3 Hz), 7.91 (1H, s), 8.27 (1H, s), 8.51 (1H, s). 130 (CDCl₃) δ 1.48-2.17 (6H, m), 2.34 (6H, s), 3.52-3.60 (1H, m), 3.92 (1H, dd, J = 2.5, 11.2 Hz), 4.11-4.18 (1H, m), 7.35 (2H, s), 7.47 (1H, t, J = 7.8 Hz), 7.60 (1H, broad), 7.69 (1H, d, J = 7.8 Hz), 7.77 (1H, dd, J = 1.0, 7.8 Hz), 8.26 (1H, s), 8.54 (1H, s). 131 δ 1.97-2.07 (2H, m), 2.15-2.31 (9H, m), 2.97-3.07 (2H, m), 3.99- 3.98 (2H, m), 7.46 (2H, s), 7.55 (1H, t, J = 8.0 Hz), 7.65 (1H, d, J = 8.0 Hz), 7.87 (1H, d, J = 8.0 Hz), 8.20 (1H, s), 9.60 (1H, s), 9.91 (1H, s). 132 (CDCl₃) δ 2.35 (6H, s), 7.16 (1H, dd, J = 3.9, 4.9 Hz), 7.36 (2H, s), 7.51 (1H, t, J = 7.8 Hz), 7.59 (1H, dd, J = 1.0, 4.9 Hz), 7.67 (1H, dd, J = 1.0, 3.9 Hz), 7.70-7.74 (2H, m), 7.80-7.83 (1H, m), 7.95 (1H, s), 8.27 (1H, s). 133 δ 2.30 (6H, s), 7.45 (2H, s), 7.54 (1H, t, J = 8.0 Hz), 7.67 (2H, d, J = 2.4 Hz), 7.75 (1H, d, J = 7.8 Hz), 8.07 (1H, d, J = 7.8 Hz), 8.31 (1H, s), 8.41 (1H, t, J = 2.2 Hz), 9.99 (1H, s), 10.28 (1H, s). 134 δ 2.30 (6H, s), 2.47 (3H, s), 7.04 (1H, d, J = 4.2 Hz), 7.45 (2H, s), 7.52 (1H, t, J = 7.8 Hz), 7.69 (1H, d, J = 4.2 Hz), 7.74 (1H, d, J = 7.8 Hz), 7.93 (1H, d, J = 7.8 Hz), 8.27 (1H, s), 9.97 (1H, s), 10.17 (1H, s). 135 δ 2.30 (6H, s), 7.45 (2H, s), 7.56 (1H, t, J = 7.8 Hz), 7.79 (1H, d, J = 7.8 Hz), 8.08 (1H, d, J = 7.8 Hz), 8.30 (1H, s), 8.71 (1H, d, J = 2.0 Hz), 8.74 (1H, d, J = 2.0 Hz), 10.01 (1H, s), 10.54 (1H, s). 136 δ 2.30 (6H, s), 2.50 (3H, s), 6.94 (1H, d, J = 3.4 Hz), 7.45 (2H, s), 7.52 (1H, t, J = 7.9 Hz), 7.74 (1H, d, J = 7.9 Hz), 7.88 (1H, d, J = 3.4 Hz), 8.02 (1H, d, J = 7.9 Hz), 8.27 (1H, s), 9.97 (1H, s), 10.32 (1H, s). 137 δ 2.29 (6H, s), 7.22 (1H, d, J = 5.1 Hz), 7.43 (2H, s), 7.53 (1H, t, J = 8.0 Hz), 7.76 (1H, d, J = 8.0 Hz), 7.91-7.93 (2H, m), 8.26 (1H, s), 9.98 (1H, s), 10.42 (1H, s). 138 δ 2.30 (6H, s), 7.45 (2H, s), 7.57 (1H, t, J = 8.1 Hz), 7.79 (1H, d, J = 8.1 Hz), 8.05 (1H, d, J = 8.1 Hz), 8.52 (1H, s), 9.97 (1H, s), 11.11 (1H, s). 139 δ 2.30 (6H, s), 7.26 (1H, d, J = 5.4 Hz), 7.45 (2H, s), 7.54 (1H, t, J = 8.0 Hz), 7.77 (1H, d, J = 8.0 Hz), 7.90-7.94 (2H, m), 8.27 (1H, s), 9.99 (1H, s), 10.50 (1H, s). 140 δ 2.30 (6H, s), 7.39 (1H, d, J = 4.6 Hz), 7.45 (2H, s), 7.54 (1H, t, J = 8.1 Hz), 7.77 (1H, d, J = 8.1 Hz), 7.92 (1H, d, J = 4.6 Hz), 8.02 (1H, d, J = 8.1 Hz), 8.26 (1H, s), 9.99 (1H, s), 10.50 (1H, s). 141 δ 2.30 (6H, s), 7.29 (1H, d, J = 4.9 Hz), 7.45 (2H, s), 7.55 (1H, t, J = 7.9 Hz), 7.77 (1H, d, J = 7.9 Hz), 7.81 (1H, d, J = 4.9 Hz), 7.92 (1H, d, J = 7.9 Hz), 8.29 (1H, s), 10.00 (1H, s), 10.50 (1H, s). 142 δ 2.27 (6H, s), 7.25-7.52 (10H, m), 7.70-7.73 (1H, m), 7.81-7.20 (1H, m), 8.12 (1H, s), 9.94 (1H, s), 10.27 (1H, s). 143 δ 2.28 (6H, s), 2.40 (3H, s), 2.45 (3H, s), 6.74 (1H, s), 7.43 (2H, s), 7.49 (1H, t, J = 8.1 Hz), 7.71 (1H, d, J = 8.1 Hz), 7.90 (1H, d, J = 8.1 Hz), 8.24 (1H, s), 9.94 (1H, s), 9.98 (1H, s). 144 δ 2.31 (6H, s), 7.41-7.59 (5H, m), 7.78 (1H, d, J = 7.8 Hz), 8.00- 8.09 (3H, m), 8.34 (1H, d, J = 2.0 Hz), 8.43 (1H, s), 10.02 (1H, s), 10.75 (1H, s). 146 δ 0.86 (3H, 7.2), 2.30 (6H, s), 4.34 (2H, q, J = 7.2 Hz), 7.45 (2H, s), 7.77-7.79 (3H, m), 7.84 (1H, s), 8.24 (1H, s), 8.37 (1H, s), 10.05 (1H, s), 11.11 (1H, s). 147 δ 2.30 (6H, s), 3.89 (3H, s), 7.45 (2H, s), 7.52 (1H, t, J = 7.9 Hz), 7.73 (1H, d, J = 7.9 Hz), 7.97 (1H, d, J = 7.9 Hz), 8.23 (1H, s), 8.45 (1H, s), 9.98 (1H, s), 10.08 (1H, s). 148 δ 2.35 (6H, s), 3.92 (3H, s), 7.26 (1H, s), 7.36 (2H, s), 7.48-7.55 (2H, m),, 7.70 (1H, d, J = 7.7 Hz), 7.83 (1H, d, J = 7.7 Hz), 8.26 (1H, s), 8.47 (1H, s). 149 δ 2.36 (6H, s), 3.95 (3H, s), 7.26 (1H, s), 7.36 (2H, s), 7.50 (1H, t, J = 7.7 Hz), 7.70 (1H, d, J = 7.7 Hz), 7.83 (1H, d, J = 7.7 Hz), 8.00 (1H, s), 8.26 (1H, s), 8.58 (1H, s). 150 (CDCl₃) δ 2.35 (6H, s), 4.01 (3H, s), 7.36 (2H, s), 7.51 (1H, t, J = 7.8 Hz), 7.68-7.73 (3H, m), 7.92 (1H, s), 8.05 (1H, s), 8.25 (1H, s). 151 δ 2.29 (6H, s), 4.06 (3H, s), 7.44 (2H, s), 7.53 (1H, t, J = 7.9 Hz), 7.77 (1H, d, J = 7.9 Hz), 7.96 (1H, d, J = 7.9 Hz), 8.11 (1H, s), 8.26 (1H, s), 10.02 (1H, s), 10.58 (1H, s). 152 δ 2.30 (6H, s), 7.32 (1H, d, J = 2.0 Hz), 7.45 (2H, s), 7.58 (1H, t, J = 7.8 Hz), 7.81 (1H, d, J = 7.8 Hz), 8.04 (1H, d, J = 7.8 Hz), 8.35 (1H, s), 8.84 (1H, d, J = 2.0 Hz), 10.03 (1H, s), 10.97 (1H, s). 153 δ 2.29 (6H, s), 7.46 (2H, s), 7.64 (1H, t), 7.72 (1H, d, J = 1.0 Hz), 7.81 (1H, s), 7.97 (1H, d, J = 8.0 Hz), 8.17 (1H, s), 8.34 (1H, s), 10.04 (1H, s). 154 δ 2.29 (6H, s), 2.51 (3H, s), 2.56 (3H, s), 7.46 (2H, s), 7.53 (1H, t, J = 8.03 Hz), 7.75 (1H, d, J = 8.03 Hz), 7.92 (1H, d, J = 8.03 Hz), 8.24 (1H, s), 9.79 (1H, s), 10.30 (1H, s). 155 δ 1.36 (3H, t, J = 7.3 Hz), 2.30 (6H, s), 2.73 (3H, s), 3.05 (2H, q, J = 7.3 Hz), 7.45 (2H, s), 7.55 (1H, t, J = 8.3 Hz), 7.78 (1H, d, J = 8.3 Hz), 7.98 (1H, d, J = 8.3 Hz), 8.29 (1H, s), 10.01 (1H, s), 10.69 (1H, s). 156 δ 2.28 (6H, s), 2.57 (3H, s), 7.43 (2H, s), 7.53 (1H, t, J = 7.8 Hz), 7.77 (1H, d, J = 7.8 Hz), 7.91 (1H, d, J = 7.8 Hz), 8.21 (1H, s), 9.98 (1H, s), 10.47 (1H, s). 157 δ 2.31 (6H, s), 7.45 (2H, s), 7.57 (1H, t, J = 7.8 Hz), 7.79 (1H, d, J = 7.8 Hz), 8.06 (1H, d, J = 7.8 Hz), 8.53 (1H, s), 10.00 (1H, s), 11.12 (1H, s). 158 δ 2.36 (6H, s), 7.45 (2H, s), 7.57 (1H, t, J = 8.1 Hz), 7.79 (1H, d, J = 8.1 Hz), 8.06 (1H, d, J = 8.1 Hz), 8.53 (1H, s), 10.01 (1H, s), 11.11 (1H, s). 159 δ 2.30 (6H, s), 7.45 (2H, s), 7.56-7.66 (3H, m), 7.80 (1H, d, J = 8.3 Hz), 7.94-7.98 (2H, m), 8.16-8.20 (1H, m), 8.32 (1H, s), 10.04 (1H, s), 10.79 (1H, s). 160 δ 2.31 (6H, s), 7.45 (2H, s), 7.53-7.61 (2H, m), 7.78 (1H, d, J = 7.8 Hz), 7.92-7.95 (1H, m), 8.02-8.07 (2H, m), 8.34 (1H, s), 9.99 (1H, s), 10.50 (1H, s). 161 δ 2.30 (6H, s), 7.37 (1H, t, J = 7.8 Hz), 7.45 (2H, s), 7.57 (1H, t, J = 7.8 Hz), 7.62-7.65 (2H, m), 7.79 (1H, d, J = 7.8 Hz), 7.99 (1H, d, J = 7.8 Hz), 8.30 (1H, s), 10.01 (1H, s), 10.65 (1H, s). 163 δ 2.38 (3H, s), 7.53-7.63 (4H, m), 7.70 (1H, s), 7.77 (1H, d, J = 7.8 Hz), 7.81 (1H, s), 7.99-8.01 (2H, m), 8.08 (1H, d, J = 7.8 Hz), 8.37 (1H, s), 10.28 (1H, s), 10.50 (1H, s). 164 (CDCl₃) δ 1.20 (3H, t, J = 7.3 Hz), 2.32 (3H, s), 2.67 (2H, q, J = 7.3 Hz), 7.36 (2H, s), 7.46-7.51 (3H, m), 7.55-7.59 (1H, m), 7.67-7.72 (2H, m), 7.85-7.88 (3H, m), 8.15 (1H, s), 8.28 (1H, s). 165 δ 1.13 (3H, t, J = 7.3 Hz), 2.29 (3H, s), 2.67 (2H, q, J = 7.3 Hz), 7.33-7.41 (3H, m), 7.47 (1H, s), 7.52-7.63 (2H, m), 7.67-7.76 (2H, m), 7.97 (1H, d, J = 7.8 Hz), 8.32 (1H, s), 10.01 (1H, s), 10.65 (1H, s). 166 δ 2.36 (3H, s), 7.53-7.63 (4H, m), 7.68 (1H, s), 7.79 (1H, d, J = 7.8 Hz), 7.96 (1H, s), 7.99-8.01 (2H, m), 8.08 (1H, dd, J = 1.5, 7.8 Hz), 8.38 (1H, d, J = 1.5 Hz), 10.27 (1H, s), 10.50 (1H, s). 167 (CDCl₃) δ 2.48 (3H, s), 7.05 (1H, s), 7.23 (1H, s), 7.50-7.62 (4H, m), 7.69 (1H, d, J = 7.8 Hz), 7.84 (1H, dd, J = 2.0, 7.8 Hz), 7.89 (2H, d, J = 6.8 Hz), 8.13 (1H, s), 8.16 (1H, d, J = 6.8 Hz), 8.39 (1H, t, J = 1.9 Hz), 8.89 (1H, s). 168 δ 1.15 (3H, t, J = 7.3 Hz), 2.73 (2H, q, J = 7.3 Hz), 7.50-7.63 (5H, m), 7.71-7.77 (2H, m), 7.94-8.01 (2H, m), 8.08 (1H, d, J = 7.8 Hz), 8.37 (1H, s), 10.28 (1H, s), 10.50 (1H, s). 169 δ 1.14 (3H, t, J = 7.3 Hz), 2.73 (2H, q, J = 7.3 Hz), 7.52-7.64 (5H, m), 7.76 (1H, d, J = 7.8 Hz), 7.83 (1H, d, J = 2.0 Hz), 7.98-8.01 (2H, m), 8.06-8.09 (1H, m), 8.37 (1H, s), 10.29 (1H, s), 10.48 (1H, s). 170 δ 1.14 (3H, t, J = 7.3 Hz), 2.72 (2H, q, J = 7.3 Hz), 7.33-7.39 (2H, m), 7.53-7.64 (3H, m), 7.67-7.72 (1H, m), 7.76 (1H, d, J = 7.8 Hz), 7.82 (1H, s), 7.98 (1H, d, J = 8.8 Hz), 8.32 (1H, s), 10.30 (1H, s), 10.65 (1H, s). 171 δ 1.13 (3H, t, J = 7.3 Hz), 2.71 (2H, q, J = 7.3 Hz), 7.52-7.63 (5H, m), 7.78 (1H, d, J = 7.8 Hz), 7.97-8.01 (3H, m), 8.07-8.09 (1H, m), 8.37 (1H, d, J = 2.0 Hz), 10.28 (1H, s), 10.48 (1H, s). 172 δ 1.13 (3H, t, J = 7.3 Hz), 2.71 (2H, q, J = 7.3 Hz), 7.33-7.39 (2H, m), 7.54-7.63 (3H, m), 7.67-7.72 (1H, m), 7.78 (1H, d, J = 7.8 Hz), 7.97-8.00 (2H, m), 8.33 (1H, s), 10.30 (1H, s), 10.66 (1H, s). 173 δ 1.13 (3H, t, J = 7.3 Hz), 2.72 (2H, q, J = 7.3 Hz), 7.57-7.64 (2H, m), 7.83 (1H, d, J = 7.8 Hz), 7.98 (1H, s), 8.10 (1H, d, J = 7.8 Hz), 8.24 (2H, d, J = 8.8 Hz), 8.37 (1H, s), 8.40 (2H, d, J = 8.8 Hz), 10.32 (1H, s), 10.81 (1H, s). 174 δ 1.13 (3H, t, J = 7.3 Hz), 2.71 (2H, q, J = 7.3 Hz), 7.56-7.63 (2H, m), 7.82 (1H, d, J = 7.8 Hz), 7.98 (1H, s), 8.04-8.10 (3H, m), 8.15 (2H, d, J = 8.3 Hz), 8.36 (1H, s), 10.31 (1H, s), 10.72 (1H, s). 175 δ 0.85 (3H, t, J = 7.3 Hz), 1.49-1.59 (2H, m), 2.30 (3H, s), 2.65 (2H, t, J = 6.8 Hz), 7.40 (1H, s), 7.47 (1H, s), 7.58 (1H, t, J = 7.8 Hz), 7.79 (1H, d, J = 7.8 Hz), 8.08 (1H, s), 8.22-8.25 (2H, m), 8.36- 8.41 (3H, m), 10.03 (1H, s), 10.79 (1H, s). 176 δ 1.18 (6H, d, J = 6.8 Hz), 2.29 (3H, s), 3.23 (1H, septet, J = 6.8 Hz), 7.41 (1H, s), 7.47 (1H, s), 7.52-7.63 (4H, m), 7.75 (1H, d, J = 7.8 Hz), 7.99-8.01 (2H, m), 8.06-8.09 (1H, m), 8.36 (1H, t, J = 2.0 Hz), 10.00 (1H, s), 10.48 (1H, s). 177 δ 1.17 (6H, d, J = 6.8 Hz), 2.30 (3H, s), 3.24 (1H, septet, J = 6.8 Hz), 7.28-7.41 (3H, m), 7.47 (1H, s), 7.55-7.63 (2H, m), 7.65-7.78 (2H, m), 7.99 (1H, d, J = 7.8 Hz), 8.33 (1H, s), 10.02 (1H, s), 10.66 (1H, s). 178 δ 0.85 (3H, t, J = 7.3 Hz), 1.47-1.60 (2H, m), 2.70 (2H, t, J = 7.3 Hz), 7.53-7.63 (5H, m), 7.75 (1H, d, J = 7.8 Hz), 7.83 (1H, d, J = 2.0 Hz), 7.98-8.01 (2H, m), 8.08 (1H, d, J = 7.8 Hz), 8.36 (1H, s), 10.29 (1H, s),10.49 (1H, s). 179 δ 0.85 (3H, t, J = 7.3 Hz), 1.50-1.60 (2H, m), 2.69 (2H, t, J = 6.8 Hz), 7.29-7.40 (2H, m), 7.53-7.62 (3H, m), 7.67-7.76 (2H, m), 7.83 (1H, d, J = 2.0 Hz), 7.98 (1H, d, J = 7.8 Hz), 8.32 (1H, s), 10.31 (1H, s), 10.66 (1H, s). 180 δ 0.85 (3H, t, J = 7.3 Hz), 1.50-1.58 (2H, m), 2.70 (2H, t, J = 7.8 Hz), 7.57-7.63 (2H, m), 7.78-7.84 (2H, m), 8.09 (1H, d, J = 7.8 Hz), 8.18-8.24 (2H, m), 8.35-8.41 (3H, m), 10.32 (1H, s), 10.80 (1H, s). 181 δ 0.85 (3H, t, J = 7.3 Hz), 1.50-1.60 (2H, m), 2.69 (2H, t, J = 7.3 Hz), 7.56-7.62 (2H, m), 7.79 (1H, d, J = 7.8 Hz), 7.83 (1H, d, J = 2.0 Hz), 8.04-8.09 (3H, m), 8.15 (2H, d, J = 8.8 Hz), 8.35 (1H, s), 10.31 (1H, s), 10.72 (1H, s). 182 δ 0.84 (3H, t, J = 7.3 Hz), 1.49-1.59 (2H, m), 2.68 (2H, t, J = 7.3 Hz), 7.53-7.63 (5H, m), 7.77 (1H, d, J = 7.8 Hz), 7.97-8.01 (3H, m), 8.08 (1H, d, J = 7.8 Hz), 8.37 (1H, s), 10.29 (1H, s), 10.49 (1H, s). 183 δ 0.84 (3H, t, J = 7.3 Hz), 1.49-1.59 (2H, m), 2.67 (2H, t, J = 7.3 Hz), 7.28-7.40 (2H, m), 7.51-7.63 (3H, m), 7.68-7.72 (1H, m), 7.77 (1H, d, J = 8.3 Hz), 7.97-8.00 (2H, m), 8.33 (1H, s), 10.31 (1H, s), 10.67 (1H, s). 184 δ 0.84 (3H, t, J = 7.3 Hz), 1.49-1.59 (2H, m), 2.68 (2H, t, J = 6.8 Hz), 7.57-7.62 (2H, m), 7.82 (1H, d, J = 7.8 Hz), 7.98 (1H, d, J = 2.0 Hz), 8.08-8.10 (1H, m), 8.15-8.41 (5H, m), 10.32 (1H, s), 10.80 (1H, s). 185 δ 0.84 (3H, t, J = 7.3 Hz), 1.49-1.57 (2H, m), 2.68 (2H, broad), 7.56-7.61 (2H, m), 7.81 (1H, d, J = 7.8 Hz), 7.98 (1H, s), 8.05 (2H, d, J = 8.3 Hz), 8.09 (1H, s), 8.15 (2H, d, J = 8.3 Hz), 8.35 (1H, s), 10.31 (1H, s), 10.72 (1H, s). 186 δ 0.84 (3H, t, J = 7.3 Hz), 1.49-1.57 (2H, m), 2.68 (2H, t, J = 6.8 Hz), 7.56-7.61 (2H, m), 7.80 (1H, d, J = 7.8 Hz), 7.94 (2H, d, J = 8.3 Hz), 7.98 (1H, s), 8.09 (1H, d, J = 7.8 Hz), 8.20 (2H, d, J = 8.3 Hz), 8.36 (1H, s), 10.31 (1H, s), 10.71 (1H, s). 187 δ 0.83 (3H, t, J = 7.3 Hz), 1.21-1.31 (2H, m), 1.47-1.55 (2H, m), 2.72 (2H, t, J = 7.8 Hz), 7.53-7.63 (5H, m), 7.70-7.75 (2H, m), 7.99-8.01 (2H, m), 8.06-8.09 (1H, m), 8.37 (1H, t, J = 2.0 Hz), 10.27 (1H, s), 10.49 (1H, s). 188 δ 0.83 (3H, t, J = 7.3 Hz), 1.21-1.31 (2H, m), 1.47-1.55 (2H, m), 2.72 (2H, t, J = 7.8 Hz), 7.33-7.40 (2H, m), 7.53-7.63 (3H, m), 7.67-7.75 (3H, m), 7.98 (1H, d, J = 7.8 Hz), 8.32 (1H, s), 10.29 (1H, s), 10.66 (1H, s). 189 δ 0.83 (3H, t, J = 7.3 Hz), 1.21-1.31 (2H, m), 1.47-1.55 (2H, m), 2.72 (2H, t, J = 7.3 Hz), 7.52-7.63 (5H, m), 7.75 (1H, d, J = 7.8 Hz), 7.82 (1H, d, J = 1.5 Hz), 7.99-8.01 (2H, m), 8.08 (1H, dd, J = 1.5, 7.8 Hz), 8.37 (1H, t, J = 1.5 Hz), 10.29 (1H, s), 10.49 (1H, s). 190 δ 0.83 (3H, t, J = 7.3 Hz), 1.21-1.31 (2H, m), 1.47-1.55 (2H, m), 2.71 (2H, t, J = 7.3 Hz), 7.28-7.37 (2H, m), 7.53-7.62 (3H, m), 7.72 (1H, t, J = 7.3 Hz), 7.75 (1H, d, J = 7.8 Hz), 7.82 (1H, s), 7.98 (1H, d, J = 7.8 Hz), 8.62 (1H, s), 10.31 (1H, s), 10.66 (1H, s). 191 δ 0.82 (3H, t, J = 7.3 Hz), 1.22-1.30 (2H, m), 1.46-1.54 (2H, m), 2.70 (2H, t, J = 7.8 Hz), 7.53-7.63 (5H, m), 7.78 (1H, d, J = 7.8 Hz), 7.93-8.02 (3H, m), 8.07-8.09 (1H, m), 8.37 (1H, s), 10.29 (1H, s), 10.49 (1H, s). 192 δ 0.83 (3H, t, J = 7.3 Hz), 1.21-1.31 (2H, m), 1.47-1.55 (2H, m), 2.71 (2H, t, J = 7.8 Hz), 7.28-7.40 (2H, m), 7.55-7.65 (3H, m), 7.69-7.73 (1H, m), 7.79 (1H, d, J = 7.8 Hz), 7.98-8.02 (2H, m), 8.35 (1H, s), 10.33 (1H, s), 10.68 (1H, s). 193 δ 0.75 (3H, t, J = 7.3 Hz), 1.18 (3H, d, J = 6.8 Hz), 1.55-1.60 (2H, m), 3.00-3.05 (1H, m), 7.49-7.67 (5H, m), 7.72-7.77 (2H, m), 7.99- 8.02 (2H, m), 8.09 (1H, d, J = 7.8 Hz), 8.36 (1H, s), 10.29 (1H, s), 10.49 (1H, s). 194 δ 0.75 (3H, t, J = 7.3 Hz), 1.17 (3H, d, J = 6.8 Hz), 1.55-1.60 (2H, m), 2.98-3.04 (1H, m), 7.52-7.63 (5H, m), 7.77 (1H, d, J = 8.3 Hz), 7.84 (1H, s), 7.99-8.10 (3H, m), 8.36 (1H, s), 10.30 (1H, s), 10.49 (1H, s). 195 δ 0.74 (3H, t, J = 7.3 Hz), 1.17 (3H, d, J = 6.8 Hz), 1.55-1.63 (2H, m), 2.98-3.04 (1H, m), 7.33-7.40 (2H, m), 7.52-7.63 (3H, m), 7.67- 7.77 (2H, m), 7.83 (1H, d, J = 1.5 Hz), 7.99 (1H, d, J = 8.3 Hz), 8.32 (1H, s), 10.32 (1H, s), 10.66 (1H, s). 196 δ 0.74 (3H, t, J = 6.8 Hz), 1.15 (3H, d, J = 6.8 Hz), 1.53-1.64 (2H, m), 2.94-3.04 (1H, m), 7.51-7.63 (5H, m), 7.79 (1H, d, J = 7.3 Hz), 7.98-8.02 (3H, m), 8.09 (1H, dd, J = 1.5, 7.8 Hz), 8.37 (1H, s), 10.30 (1H, s), 10.50 (1H, s). 197 δ 7.33-7.41 (2H, m), 7.56-7.64 (2H, m), 7.68-7.73 (2H, m), 7.93- 8.03 (2H, m), 8.38-8.40 (1H, m), 8.45 (1H, d, J = 2.0 Hz), 10.72 (1H, s), 10.98 (1H, s). 198 δ 2.50 (3H, s), 7.39 (1H, s), 7.48-7.63 (4H, m), 7.73 (1H, s), 7.77 (1H, d, J = 7.8 Hz), 7.99-8.01 (2H, m), 8.08 (1H, d, J = 7.8 Hz), 8.35 (1H, s), 10.36 (1H, s), 10.50 (1H, s). 199 δ 2.50 (3H, s), 7.33-7.39 (3H, m), 7.53-7.63 (2H, m), 7.67-7.77 (3H, m), 7.98 (1H, d, J = 7.8 Hz), 8.30 (1H, s), 10.38 (1H, s), 10.67 (1H, s). 200 δ 2.81 (3H, s), 7.53-7.64 (4H, m), 7.75 (1H, d, J = 8.3 Hz), 7.99- 8.01 (2H, m), 8.08-8.11 (2H, m), 8.25 (1H, d, J = 2.0 Hz), 8.40 (1H, t, J = 2.0 Hz), 10.52 (1H, s), 10.61 (1H, s). 201 δ 3.40 (3H, s), 7.33-7.40 (2H, m), 7.56-7.63 (2H, m), 7.67-7.78 (2H, m), 7.99 (1H, d, J = 8.3 Hz), 8.17 (1H, d, J = 1.5 Hz), 8.35 (1H, s), 8.39 (1H, d, J = 1.5 Hz), 10.63 (1H, s), 10.69 (1H, s). 202 δ 3.40 (3H, s), 7.57-7.62 (2H, m), 7.79 (1H, d, J = 7.8 Hz), 7.96 (1H, dd, J = 1.5, 8.3 Hz), 8.12 (1H, dd, J = 1.5, 8.3 Hz), 8.17 (1H, d, J = 2.0 Hz), 8.32 (1H, d, J = 2.0 Hz), 8.40 (1H, d, J = 2.0 Hz), 8.54-8.56 (1H, m), 10.65 (1H, s), 10.92 (1H, s). 203 δ 3.40 (3H, s), 7.53-7.63 (4H, m), 7.78 (1H, d, J = 7.8 Hz), 7.98- 8.01 (2H, m), 8.07-8.10 (1H, m), 8.21 (1H, s), 8.39 (1H, s), 8.48 (1H, d, J = 1.5 Hz), 10.51 (1H, s), 10.63 (1H, s). 204 δ 3.39 (3H, s), 7.33-7.40 (2H, m), 7.56-7.63 (2H, m), 7.68-7.72 (1H, m), 7.78 (1H, d, J = 7.8 Hz), 8.00 (1H, d, J = 7.8 Hz), 8.21 (1H, d, J = 1.5 Hz), 8.35 (1H, s), 8.48 (1H, d, J = 1.5 Hz), 10.66 (1H, s), 10.69 (1H, s). 205 δ 3.39 (3H, s), 7.36-7.42 (2H, m), 7.58 (1H, t, J = 7.8 Hz), 7.78 (1H, d, J = 7.8 Hz), 8.06-8.10 (3H, m), 8.21 (1H, s), 8.36 (1H, s), 8.48 (1H, s), 10.52 (1H, s), 10.63 (1H, s). 206 δ 3.39 (3H, s), 7.61 (1H, t, J = 7.8 Hz), 7.82 (1H, d, J = 7.8 Hz), 8.09 (1H, d, J = 7.8 Hz), 8.20-8.24 (3H, m), 8.37-8.41 (3H, m), 8.48 (1H, s), 10.67 (1H, s), 10.83 (1H, s). 207 δ 3.39 (3H, s), 7.60 (1H, t, J = 7.8 Hz), 7.81 (1H, d, J = 7.8 Hz), 7.97-8.10 (3H, m), 8.14-8.21 (3H, m), 8.37 (1H, t, J = 2.0 Hz), 8.48 (1H, d, J = 2.0 Hz), 10.65 (1H, s), 10.74 (1H, s). 208 δ 3.39 (3H, s), 7.57-7.62 (2H, m), 7.80 (1H, d, J = 7.8 Hz), 7.96 (1H, dd, J = 1.5, 7.8 Hz), 8.11 (1H, dd, J = 1.5, 7.8 Hz), 8.20 (1H, s), 8.31 (1H, s), 8.51 (1H, s), 8.55 (1H, dd, J = 1.5, 4.9 Hz), 10.68 (1H, s), 10.92 (1H, s). 209 δ 1.96 (3H, s), 3.84 (2H, broad), 7.53-7.63 (4H, m), 7.73 (1H, d, J = 7.8 Hz), 7.89 (1H, s), 7.99-8.01 (2H, m), 8.07 (1H, dd, J = 1.5, 7.8 Hz), 8.19 (1H, s), 8.33 (1H, t, J = 2.0 Hz), 10.43 (1H, s), 10.49 (1H, s). 210 δ 7.53-7.64 (4H, m), 7.81 (1H, d, J = 7.8 Hz), 8.00-8.05 (3H, m), 8.11 (1H, d, J = 7.8 Hz), 8.31 (1H, d, J = 1.5 Hz), 8.41 (1H, s), 10.52 (1H, s), 10.93 (1H, s). 211 δ 2.29 (6H, s), 7.47 (2H, s), 7.50-7.62 (4H, m), 7.75 (1H, d, J = 7.8 Hz), 7.97-8.00 (2H, m), 8.05 (1H, dd, J = 1.5, 7.8 Hz), 8.36 (1H, s), 10.01 (1H, s), 10.46 (1H, s). 212 δ 2.30 (6H, s), 7.45 (2H, s), 7.51-7.63 (4H, m), 7.76 (1H, d, J = 7.8 Hz), 7.98-8.07 (3H, m), 8.37 (1H, d, J = 2.0 Hz), 9.99 (1H, s), 10.48 (1H, s). 255 δ 7.25-7.29 (2H, m), 7.54-7.65 (2H, m), 7.78 (1H, d, J = 7.8 Hz), 7.92-7.95 (1H, m), 8.03 (2H, s), 8.30 (1H, s), 10.58 (1H, s), 11.05 (1H, s). 256 δ 7.53-7.63 (4H, m), 7.78 (1H, d, J = 7.3 Hz), 7.99-8.01 (2H, m), 8.06-8.09 (1H, m), 8.17 (2H, s), 8.38 (1H, s), 10.50 (1H, s), 10.55 (1H, s). 257 δ 7.25-7.29 (2H, m), 7.55-7.63 (2H, m), 7.79 (1H, d, J = 7.3 Hz), 7.94 (1H, d, J = 8.3 Hz), 8.17 (2H, s), 8.30 (1H, s), 10.60 (1H, s), 11.05 (1H, s). 258 (CDCl₃) δ 7.45-7.61 (4H, m), 7.76 (1H, d, J = 7.8 Hz), 7.84-7.91 (3H, m), 7.93 (2H, s), 8.02 (1H, s), 8.08 (1H, d, J = 6.8 Hz), 8.31 (1H, s). 259 (CDCl₃) δ 7.22 (1H, dd, J = 7.8, 12.2 Hz), 7.35 (1H, t, J = 7.8 Hz), 7.52-7.60 (2H, m), 7.77 (1H, d, J = 7.8 Hz), 7.88 (1H, s), 7.92 (1H, s), 7.93 (2H, d), 8.19 (1H, dt, J = 1.9, 7.8 Hz), 8.33 (1H, s), 8.64 (1H, d, J = 15.6 Hz). 260 (CDCl₃) δ 2.31 (6H, s), 7.41 (2H, s), 7.50-7.67 (5H, m), 7.71 (1H, d, J = 7.8 Hz), 7.87-7.90 (3H, m), 8.07 (1H, s), 8.31 (1H, s). 261 (CDCl₃) δ 2.33 (6H, s), 7.20-7.25 (1H, m), 7.35 (1H, t, J = 7.3 Hz), 7.44 (2H, s), 7.52-7.60 (3H, m), 7.73 (1H, d, J = 7.8 Hz), 7.88 (1H, dd, J = 1.0, 7.8 Hz), 8.18 (1H, dt, J = 2.0, 7.8 Hz), 8.33 (1H, s), 8.63 (1H, d, J = 7.3 Hz). 262 (CDCl₃) δ 7.44-7.57 (5H, m), 7.72 (2H, s), 7.78 (1H, d, J = 7.8 Hz), 8.00 (1H, d, J = 6.8 Hz), 8.18 (1H, d, J = 8.3 Hz), 8.34 (1H, t, J = 2.0 Hz), 9.46 (1H, s), 9.83 (1H, s). 263 (CDCl₃) δ 7.47-7.57 (4H, m), 7.78 (1H, d, J = 7.8 Hz), 7.93 (2H, s), 7.99-8.01 (2H, m), 8.18 (1H, d, J = 7.8 Hz), 8.33 (1H, t, J = 2.0 Hz), 9.27 (1H, s), 9.65 (1H, s). 266 δ 7.20-7.25 (1H, m), 7.35 (1H, t, J = 7.8 Hz), 7.53-7.60 (2H, m), 7.76-7.79 (2H, m), 7.95 (2H, s), 7.96 (1H, s), 8.19 (1H, dt, J = 2.0, 7.8 Hz), 8.32 (1H, s), 8.63 (1H, d, J = 15.7 Hz). 276 (CDCl₃) δ 7.56 (1H, t, J = 7.8 Hz), 7.71 (1H, d, J = 7.8 Hz), 7.75 (1H, d, J = 7.8 Hz), 7.87-7.90 (3H, m), 8.04 (1H, d, J = 7.8 Hz), 8.28 (2H, s), 8.42 (1H, dd, J = 1.0, 7.3 Hz), 8.46 (1H, s), 8.76 (1H, t, J = 2.0 Hz). 284 (CDCl₃) δ 7.03 (2H, t, J = 7.8 Hz), 7.42-7.49 (1H, m), 7.54 (1H, t, J = 7.8 Hz), 7.78 (1H, d, J = 7.8 Hz), 7.81 (1H, s), 7.87-7.92 (2H, m), 7.93 (2H, s), 8.28 (1H, t, J = 2.0 Hz). 285 δ 6.86 (1H, d, J = 8.8 Hz), 7.24 (1H, t, J = 7.8 Hz), 7.30-7.32 (2H, m), 7.47 (1H, t, J = 7.8 Hz), 7.77 (1H, d, J = 7.8 Hz), 7.93 (2H, s), 8.14 (1H, d, J = 7.3 Hz), 8.31 (1H, s), 9.32 (1H, s), 9.46 (1H, s). 286 δ 2.17 (3H, s), 7.40 (1H, t, J = 7.8 Hz), 7.49 (1H, t, J = 7.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.78 (1H, d, J = 7.8 Hz), 7.94-7.95 (3H, m), 8.06 (1H, s), 8.16 (1H, d, J = 7.8 Hz), 8.31 (1H, s), 9.50 (1H, s), 9.58 (1H, s), 9.79 (1H, s). 287 δ 3.00 (3H, s), 7.42 (1H, t, J = 7.8 Hz), 7.50 (1H, t, J = 7.8 Hz), 7.48 (1H, s), 7.74 (1H, d, J = 7.8 Hz), 7.79 (1H, d, J = 7.8 Hz), 7.88 (1H, t, J = 2.0 Hz), 7.93 (2H, s), 8.17 (1H, d, J = 7.8 Hz), 8.29 (1H, t, J = 2.0 Hz), 9.37 (1H, s), 9.49 (1H, s), 9.72 (1H, s). 288 (CDCl₃) δ 7.51 (1H, t, J = 7.8 Hz), 7.69 (1H, d, J = 7.8 Hz), 7.86- 7.91 (3H, m), 7.95 (2H, s), 8.07 (1H, s), 8.39 (1H, s), 8.53-8.55 (1H, m), 8.90 (1H, s). 289 (CDCl₃) δ 7.54 (1H, t, J = 8.3 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.94 (2H, s), 8.02 (1H, d, J = 8.3 Hz), 8.26-8.27 (2H, m), 8.52 (1H, d, J = 8.3 Hz), 8.74 (1H, s), 8.87 (1H, s), 10.56 (1H, s). 290 δ 2.68 (3H, s), 7.52 (1H, t, J = 7.8 Hz), 7.81 (1H, d, J = 7.8 Hz), 7.93 (2H, s), 8.03 (2H, s), 8.07 (1H, s), 8.24 (1H, d, J = 7.8 Hz), 8.29 (1H, s), 9.34 (1H, s), 10.13 (1H, s). 291 (CDCl₃) δ 4.17 (2H, s), 6.80-6.84 (1H, m), 6.98 (1H, dd, J = 7.8, 11.2 Hz), 7.33 (1H, dd, J = 2.9, 6.4 Hz), 7.51 (1H, t, J = 7.8 Hz), 7.82 (1H, d, J = 7.8 Hz), 7.94 (2H, s), 8.10 (1H, d, J = 8.2 Hz), 8.22 (1H, s), 9.06 (1H, d, J = 13.2 Hz), 9.48 (1H, s). 292 (CDCl₃) δ 7.44 (1H, dd, J = 8.8, 10.7 Hz), 7.58 (1H, t, J = 7.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.85 (1H, s), 7.95 (2H, s), 7.98 (1H, d, J = 7.8 Hz), 8.27 (1H, s), 8.43-8.47 (1H, m), 8.55 (1H, d, J = 14.2 Hz), 9.09 (1H, dd, J = 3.0, 6.4 Hz). 293 δ 2.97 (3H, s), 7.16 (1H, dd, J = 8.8, 10.8 Hz), 7.49 (1H, t, J = 7.8 Hz), 7.51 (1H, s), 7.83 (1H, d, J = 7.8 Hz), 7.90-7.93 (1H, m), 7.94 (2H, s), 8.10 (1H, d, J = 7.8 Hz), 8.24 (1H, s), 9.15 (1H, d, J = 11.2 Hz), 9.38 (1H, s), 9.58 (1H, s). 294 (CDCl₃) δ 4.22 (3H, s), 7.56 (1H, t, J = 7.8 Hz), 7.75 (1H, t, J = 7.8 Hz), 7.83 (1H, s), 7.94 (1H, s), 7.95 (2H, s), 7.99-8.05 (2H, m), 8.25 (1H, s), 8.47 (1H, d, J = 7.8 Hz), 9.83 (1H, s). 295 δ 4.06 (3H, s), 7.52 (1H, t, J = 7.3 Hz), 7.73 (1H, d, J = 8.3 Hz), 7.82-7.88 (2H, m), 7.89 (1H, d, J = 8.3 Hz), 7.93 (2H, s), 8.25-8.29 (2H, m), 9.48 (1H, s), 10.23 (1H, s). 296 (CDCl₃) δ 2.16 (3H, s), 7.14 (1H, dd, J = 9.3, 11.2 Hz), 7.52 (1H, t, J = 7.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.94 (2H, s), 7.96 (1H, d, J = 2.9 Hz), 8.01 (1H, d, J = 7.8 Hz), 8.13-8.16 (1H, m), 8.27 (1H, s), 8.86 (1H, s), 8.90 (1H, d, J = 14.2 Hz), 9.00 (1H, s). 306 (CDCl₃) δ 7.52-7.58 (2H, m), 7.77 (1H, d, J = 7.8 Hz), 7.90 (1H, s), 7.94 (2H, s), 7.95 (1H, d, J = 7.8 Hz), 8.01-8.03 (1H, m), 8.31 (1H, d, J = 7.8 Hz), 8.47 (1H, s), 8.65 (1H, dd, J = 1.0, 4.9 Hz), 10.25 (1H, s). 307 (CDCl₃) δ 7.57 (1H, t, J = 7.8 Hz), 7.73-7.77 (3H, m), 7.84 (1H, s), 7.89 (2H, s), 8.05 (1H, d, J = 7.8 Hz), 8.26 (1H, s), 8.32 (1H, s), 8.81 (1H, s), 8.83 (1H, s). 309 (CDCl₃) δ 7.44 (1H, dd, J = 4.8, 7.8 Hz), 7.56 (1H, t, J = 7.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.86 (1H, s), 7.92 (1H, d, J = 7.3 Hz), 7.95 (2H, s), 8.23 (1H, dd, J = 20., 7.9 Hz), 8.30 (1H, s), 8.41 (1H, s), 8.55 (1H, dd, J = 2.0, 4.5 Hz). 310 (CDCl₃) δ 7.46 (1H, d, J = 8.3 Hz), 7.55 (1H, t, J = 8.3 Hz), 7.74 (1H, d, J = 8.3 Hz), 7.88 (3H, s), 8.03 (1H, d, J = 7.8 Hz), 8.18 (1H, dd, J = 3.0, 8.2 Hz), 8.24 (1H, s), 8.41 (1H, s), 8.90 (1H, d, J = 2.4 Hz). 312 (CDCl₃) δ 7.57 (1H, t, J = 7.8 Hz), 7.70 (2H, s), 7.75 (1H, d, J = 7.8 Hz), 7.83 (1H, s), 7.88 (2H, s), 8.04 (1H, d, J = 7.8 Hz), 8.21 (1H, s), 8.47 (1H, s). 313 (CDCl₃) δ 7.33 (1H, t, J = 7.8 Hz), 7.46 (1H, d, J = 8.3 Hz), 7.60 (1H, s), 7.76 (1H, s), 7.80 (1H, d, J = 7.8 Hz), 7.95 (2H, s), 8.18- 8.23 (2H, m), 8.40 (1H, s). 314 (CDCl₃) δ 2.62 (3H, s), 7.29 (1H, s), 7.56 (1H, t, J = 7.8 Hz), 7.77- 7.79 (2H, m), 7.91 (1H, s), 7.94 (2H, s), 8.16 (1H, d, J = 7.8 Hz), 8.29 (1H, s), 8.48 (1H, s). 315 (CDCl₃) δ 7.47-7.59 (3H, m), 7.80 (1H, d, J = 7.8 Hz), 7.93 (1H, s), 7.94 (2H, s), 8.26 (1H, s), 8.34 (1H, d, J = 6.5 Hz), 8.47 (1H, t, J = 2.0 Hz), 8.52-8.55 (1H, m), 13.91 (1H, s). 316 (CDCl₃) δ 7.59 (1H, t, J = 7.8 Hz), 7.79 (1H, d, J = 7.8 Hz), 7.84 (1H, s), 7.95 (2H, s), 8.04 (1H, d, J = 7.8 Hz), 8.41 (1H, t, J = 2.0 Hz), 8.63 (1H, t, J = 2.5 Hz), 8.86 (1H, d, J = 2.4 Hz), 9.54 (1H, d, J = 1.5 Hz), 9.87 (1H, s). 317 (CDCl₃) δ 3.93 (3H, s), 7.53 (1H, t, J = 7.8 Hz), 7.74 (1H, d, J = 7.8 Hz), 7.84 (1H, s), 7.87 (1H, d, J = 7.8 Hz), 7.94 (2H, s), 8.03 (1H, s), 8.26 (1H, t, J = 2.0 Hz), 8.48 (1H, s). 318 (CDCl₃) δ 4.02 (3H, s), 7.53 (1H, t, J = 7.8 Hz), 7.45 (1H, d, J = 7.8 Hz), 7.80 (1H, d, J = 7.8 Hz), 7.85 (1H, s), 7.89 (1H, s), 7.94 (2H, s), 8.05 (1H, s), 8.24 (1H, s). 319 (CDCl₃) δ 4.10 (3H, s), 7.53 (1H, t, J = 7.8 Hz), 7.67 (1H, s), 7.76 (1H, d, J = 7.8 Hz), 7.70-7.86 (3H, m), 7.94 (2H, s), 8.21 (1H, s). 320 (CDCl₃) δ 1.94-2.04 (2H, m), 2.17-2.22 (1H, m), 2.37-2.42 (1H, m), 3.95-4.00 (1H, m), 4.05-4.09 (1H, m), 4.49 (1H, dd, J = 5.9, 8.3 Hz), 7.50 (1H, t, J = 7.8 Hz), 7.72 (1H, d, J = 7.8 Hz), 7.83 (1H, dd, J = 2.0, 7.8 Hz), 7.87 (1H, s), 7.94 (2H, s), 8.23 (1H, t, J = 2.0 Hz), 8.67 (1H, s). 321 (CDCl₃) δ 7.51-7.53 (3H, m), 7.57 (1H, t, J = 8.3 Hz), 7.76 (1H, d, J = 7.3 Hz), 7.83 (1H, s), 7.95 (2H, s), 8.01-8.07 (3H, m), 8.23 (1H, s), 8.38 (1H, s), 9.51 (1H, s). 327 (CDCl₃) δ 7.45-7.61 (4H, m), 7.77 (1H, d, J = 7.8 Hz), 7.84-7.91 (3H, m), 7.97-8.18 (4H, m), 8.31 (1H, s). 328 (CDCl₃) δ 7.24 (1H, d, J = 7.8 Hz), 7.35 (1H, t, J = 7.8 Hz), 7.54- 7.60 (2H, m), 7.78 (1H, d, J = 7.8 Hz), 7.89 (1H, s), 7.96 (1H, d, J = 7.8 Hz), 8.15-8.19 (3H, m), 8.33 (1H, s), 8.64 (1H, d, J = 15.6 Hz). 329 (CDCl₃) δ 7.44-7.57 (4H, m), 7.70 (2H, s), 7.78 (1H, d, J = 7.8 Hz), 8.01 (2H, d, J = 6.8 Hz), 8.17 (1H, dd, J = 1.0, 7.8 Hz), 8.34 (1H, t, J = 2.0 Hz), 9.45 (1H, s), 9.81 (1H, s). 330 (CDCl₃) δ 7.22 (1H, dd, J = 8.3, 12.2 Hz), 7.34 (1H, t, J = 7.3 Hz), 7.52-7.67 (2H, m), 7.72 (2H, s), 7.76 (1H, d, J = 7.9 Hz), 7.90 (1H, s), 7.92 (1H, s), 8.18 (1H, dt, J = 1.4, 7.8 Hz), 8.33 (1H, t, J = 2.0 Hz), 8.64 (1H, d, J = 16.6 Hz). 331 (CDCl₃) δ 7.44 (1H, dd, J = 4.4, 7.8 Hz), 7.57 (1H, t, J = 7.8 Hz), 7.73 (2H, s), 7.78 (1H, d, J = 7.8 Hz), 7.84 (1H, s), 7.90 (1H, d, J = 7.8 Hz), 8.23 (1H, dd, J = 2.0, 7.8 Hz), 8.29 (1H, s), 8.41 (1H, s), 8.55 (1H, dd, J = 2.0, 4.9 Hz). 332 δ 7.43-7.57 (4H, m), 7.79 (1H, d, J = 7.8 Hz), 7.92 (2H, s), 8.00 (2H, d, J = 6.9 Hz), 8.18 (1H, d, J = 8.3 Hz), 8.35 (1H, t, J = 2.0 Hz), 8.59 (1H, s), 9.86 (1H, s). 333 (CDCl₃) δ 7.30-7.62 (4H, m), 7.75 (1H, d, J = 7.8 Hz), 7.84 (1H, d, J = 7.8 Hz), 7.89-7.92 (3H, m), 7.93 (2H, s), 8.03 (1H, s), 8.31 (1H, s). 334 (CDCl₃) δ 7.20-7.25 (1H, m), 7.35 (1H, t, J = 6.3 Hz), 7.54-7.58 (2H, m), 7.79 (1H, d, J = 6.3 Hz), 7.90-7.94 (2H, m), 7.95 (2H, s), 8.19 (1H, t, J = 8.3 Hz), 8.33 (1H, t, J = 2.0 Hz), 8.64 (1H, d, J = 16.1 Hz). 335 (CDCl₃) δ 7.51-7.62 (4H, m), 7.77 (1H, d, J = 7.3 Hz), 7.89-7.93 (3H, m), 8.02 (2H, s), 8.08 (1H, s), 8.26 (1H, s), 8.37 (1H, d, J = 14.6 Hz). 338 (CDCl₃) δ 7.22 (1H, t, J = 7.8 Hz), 7.36 (1H, t, J = 7.8 Hz), 7.54- 7.60 (2H, m), 7.78 (1H, d, J = 7.8 Hz), 7.90 (1H, d, J = 7.8 Hz), 8.03-8.04 (2H, m), 8.19 (1H, t, J = 7.8 Hz), 8.26 (1H, s), 8.41 (1H, s), 8.65 (1H, d, J = 16.6 Hz). 369 (CDCl₃) δ 7.46 (1H, dd, J = 4.4, 7.8 Hz), 7.59 (1H, t, J = 8.3 Hz), 7.81 (1H, d, J = 8.3 Hz), 7.89-7.92 (1H, m), 8.04 (2H, s), 8.24 (1H, dd, J = 2.0, 7.8 Hz), 8.27 (1H, s), 8.35 (1H, d, J = 13.7 Hz), 8.42 (1H, s), 8.56 (1H, dd, J = 1.4, 4.4 Hz). 375 δ 7.25 (1H, d, J = 8.3 Hz), 7.27 (1H, d, J = 7.8 Hz), 7.56-7.64 (2H, m), 7.79 (1H, d, J = 7.8 Hz), 7.94 (1H, d, J = 8.3 Hz), 8.32 (1H, s), 8.42 (2H, s), 10.87 (1H, s), 11.05 (1H, s). 376 δ 7.53-7.64 (4H, m), 7.80 (1H, d, J = 7.8 Hz), 7.99-8.01 (2H, m), 8.09 (1H, dd, J = 1.5, 7.8 Hz), 8.41 (1H, d, J = 1.5 Hz), 8.54 (2H, s), 10.52 (1H, s), 10.83 (1H, s). 377 δ 7.19-7.30 (2H, m), 7.57-7.66 (2H, m), 7.81 (1H, d, J = 7.8 Hz), 7.95 (1H, dd, J = 1.5, 7.8 Hz), 8.33 (1H, t, J = 1.5 Hz), 8.53 (2H, s), 10.89 (1H, s), 11.08 (1H, s). 378 (CDCl₃) δ 7.21-7.23 (1H, m), 7.36 (1H, t, J = 6.9 Hz), 7.55-7.59 (2H, m), 7.79 (1H, d, J = 8.3 Hz), 7.84 (1H, d, J = 8.0 Hz), 8.05 (2H, s), 8.17-8.21 (2H, m), 8.43 (1H, t, J = 2.0 Hz), 8.65 (1H, d, J = 6.9 Hz). 379 (CDCl₃) δ 7.46-7.63 (4H, m), 7.77 (1H, d, J = 7.8 Hz), 7.84-7.91 (3H, m), 8.00 (1H, s), 8.07 (2H, s), 8.14 (1H, s), 8.40 (1H, t, J = 2.0 Hz). 380 (CDCl₃) δ 7.52-7.63 (4H, m), 7.77 (1H, d, J = 7.8 Hz), 7.89 (1H, s), 7.90 (2H, d, J = 7.8 Hz), 7.99 (1H, s), 8.03 (1H, s), 8.26 (2H, s), 8.39 (1H, t, J = 2.0 Hz). 383 (CDCl₃) δ 7.21 (1H, d, J = 8.3 Hz), 7.36 (1H, t, J = 7.8 Hz), 7.55- 7.61 (2H, m), 7.78 (1H, d, J = 7.8 Hz), 7.90 (1H, d, J = 8.3 Hz), 8.02 (1H, s), 8.19 (1H, dt, J = 1.9, 8.3 Hz), 8.27 (2H, s), 8.41 (1H, s), 8.65 (1H, d, J = 16.6 Hz). 414 (CDCl₃) δ 7.44 (1H, dd, J = 4.9, 7.8 Hz), 7.59 (1H, t, J = 8.3 Hz), 7.81 (1H, d, J = 7.8 Hz), 7.89 (1H, d, J = 8.3 Hz), 8.04 (1H, s), 8.23 (1H, dd, J = 1.9, 7.8 Hz), 8.27 (2H, s), 8.37 (1H, s), 8.43 (1H, s), 8.55 (1H, dd, J = 1.9, 4.3 Hz). 460 δ 7.25 (1H, d, J = 8.3 Hz), 7.27 (1H, d, J = 7.8 Hz), 7.56-7.64 (2H, m), 7.79 (1H, d, J = 7.8 Hz), 7.94 (1H, d, J = 8.3 Hz), 8.32 (1H, s), 8.42 (2H, s), 10.87 (1H, s), 11.05 (1H, s). 461 (CDCl₃) δ 2.47 (3H, s), 7.51-7.62 (5H, m), 7.75 (1H, d, J = 7.8 Hz), 7.89-7.93 (4H, m), 8.00 (1H, broad-s), 8.35 (1H, t, J = 2.0 Hz). 462 (CDCl₃) δ 2.47 (3H, s), 7.20-7.23 (1H, m), 7.36 (1H, t, J = 7.8 Hz), 7.55-7.60 (3H, m), 7.76 (1H, d, J = 7.8 Hz), 7.89 (1H, s), 7.92 (1H, s), 8.18-8.22 (1H, m), 8.39 (1H, s), 8.62 (1H, broad-s). 463 (CDCl₃) δ 2.27 (3H, s), 2.41 (3H, s), 6.59 (1H, septet, J = 6.4 Hz), 6.72 (1H, s), 7.49-7.61 (5H, m), 7.70 (1H, d, J = 7.8 Hz), 7.83-7.89 (3H, m), 8.05 (1H, broad-s), 8.33 (1H, t, J = 1.5 Hz). 464 (CDCl₃) δ 2.38 (3H, s), 6.34 (1H, septet, J = 6.4 Hz), 6.87 (1H, s), 7.50-7.63 (5H, m), 7.72 (1H, d, J = 7.8 Hz),7.88-7.90 (3H, m), 7.99 (1H, brs), 8.31 (1H, broad-s). 465 (CDCl₃) δ 2.37 (3H, s), 6.36 (1H, septet, J = 5.9 Hz), 6.87 (1H, s), 7.50-7.61 (4H, m), 7.72-7.73 (2H, m), 7.88-7.90 (3H, m), 8.06 (1H, broad-s), 8.32 (1H, s). 466 (CDCl₃) δ 2.39 (3H, s), 6.36 (1H, septet, J = 5.9 Hz), 6.89 (1H, s), 7.20-7.25 (1H, m), 7.35 (1H, t, J = 6.8 Hz), 7.52-7.60 (2H, m), 7.70 (1H, broad-s), 7.75 (1H, d, J = 7.8 Hz), 7.89 (1H, d, J = 7.8 Hz), 8.17-8.21 (1H, m), 8.36 (1H, s), 8.64 (1H, broad-d, J = 16.1 Hz). 467 (CDCl₃) δ 2.53 (3H, s), 6.35 (1H, septet, J = 5.9 Hz), 6.83 (1H, s), 7.49-7.61 (4H, m), 7.66 (1H, s), 7.74 (1H, d, J = 8.3 Hz), 7.88-7.92 (3H, m), 8.32 (1H, broad-s), 8.33 (1H, t, J = 1.9 Hz). 601 δ 2.34 (6H, s), 7.37 (1H, t, J = 7.8 Hz), 7.45 (2H, s), 7.53-7.65 (4H, m), 7.77-7.82 (1H, m), 8.00-8.02 (2H, m), 10.10 (1H, s), 10.29 (1H, s). 602 δ 2.36 (6H, s), 2.56 (3H, s), 7.29-7.43 (7H, m), 7.55-7.57 (1H, m), 7.75-7.78 (1H, m), 7.84-7.88 (1H, m), 8.64-8.66 (1H, m). 603 δ 2.37 (6H, s), 2.46 (3H, s), 7.34-7.42 (5H, m), 7.69-7.85 (4H, m), 8.11 (1H, s), 8.59-8.63 (1H, s). 604 δ 2.38 (6H, s), 2.45 (3H, s), 7.33-7.38 (5H, m), 7.78-7.85 (4H, m), 8.10 (1H, s), 8.61-8.65 (1H, m). 605 δ 2.34 (6H, s), 7.39 (1H, t, J = 7.4 Hz), 7.44 (2H, s), 7.50-7.54 (1H, m), 7.76-7.80 (2H, m), 7.88 (1H, t, J = 7.4 Hz), 8.12 (1H, t, J = 7.4 Hz), 8.20 (1H, d, J = 1.0 Hz), 10.12 (1H, s), 10.73 (1H, s). 606 δ 2.35 (6H, s), 7.40 (1H, t, J = 7.8 Hz), 7.45 (2H, s), 7.59-7.62 (1H, m), 7.82-7.90 (2H, m), 8.44-8.50 (2H, m), 8.86 (1H, d, J = 2.0 Hz), 10.12 (1H, s), 10.72 (1H, s). 607 δ 2.34 (6H, s), 7.40 (1H, t, J = 7.8 Hz), 7.45 (2H, s), 7.57-7.62 (1H, m), 7.81-7.85 (1H, m), 8.22-8.25 (2H, m), 8.39-8.42 (2H, m), 10.12 (1H, s), 10.66 (1H, s). 609 δ 2.34 (6H, s), 7.39 (1H, t, J = 6.9 Hz), 7.45 (2H, s), 7.58 (1H, t, J = 6.9 Hz), 7.82 (1H, t, J = 6.9 Hz), 8.06 (2H, d, J = 8.8 Hz), 8.15 (2H, d, J = 8.8 Hz), 10.12 (1H, s), 10.58 (1H, s). 610 δ 2.34 (6H, s), 7.33-7.40 (3H, m), 7.45 (2H, s), 7.52-7.56 (1H, m), 7.59-7.65 (1H, m), 7.72-7.77 (1H, m), 8.00 (1H, t, J = 7.8 Hz), 10.12 (1H, s), 10.35 (1H, s). 611 δ 2.34 (6H, s), 7.38 (1H, t, J = 7.6 Hz), 7.45-7.65 (5H, m), 7.78- 7.83 (2H, m), 7.87 (1H, d, J = 7.6 Hz), 10.10 (1H, s), 10.39 (1H, s). 612 δ 2.34 (6H, s), 7.35-7.45 (5H, m), 7.55-7.59 (1H, m), 7.77-7.81 (1H, m), 8.07-8.12 (2H, m), 10.09 (1H, s), 10.32 (1H, s). 616 δ 2.34 (6H, s), 7.22-7.27 (1H, m), 7.38 (1H, t, J = 7.8 Hz), 7.46 (2H, s), 7.50-7.55 (3H, m), 7.95 (1H, d, J = 7.8 Hz), 7.99-8.03 (1H, m), 10.12 (1H, s), 10.50 (1H, s). 618 δ 2.34 (6H, s), 7.39 (1H, t, J = 7.7 Hz), 7.45 (2H, s), 7.60 (1H, t, J = 7.7 Hz), 7.83 (1H, t, J = 7.7 Hz), 7.95 (2H, d, J = 8.3 Hz), 8.20 (2H, d, J = 8.3 Hz), 10.12 (1H, s), 10.56 (1H, s). 619 δ 2.34 (6H, s), 7.38 (1H, t, J = 7.4 Hz), 7.45 (2H, s), 7.55-7.60 (3H, m), 7.81 (1H, t, J = 7.4 Hz), 8.14 (2H, d, J = 8.8 Hz), 10.11 (1H, s), 10.40 (1H, s). 620 δ 2.34 (6H, s), 3.01 (6H, s), 6.77 (2H, d, J = 9.0 Hz), 7.33 (1H, t, J = 7.0 Hz), 7.45 (2H, s), 7.52 (1H, t, J = 7.0 Hz), 7.78 (1H, t, J = 7.0 Hz), 7.90 (2H, d, J = 9.0 Hz), 9.86 (1H, s), 10.07 (1H, s). 624 δ 2.34 (6H, s), 7.23-7.28 (2H, m), 7.38 (1H, t, J = 7.8 Hz), 7.45 (2H, s), 7.52-7.64 (2H, m), 8.05-8.10 (1H, m), 10.13 (1H, s), 10.88 (1H, s). 628 δ 2.34 (6H, s), 7.37-7.42 (1H, m), 7.40 (2H, s), 7.55-7.58 (1H, m), 7.95-8.07 (2H, m), 8.21 (1H, dd, J = 8.9, 2.1 Hz), 8.30 (1H, dd, J = 8.9, 2.1 Hz), 10.13 (1H, s), 10.75 (1H, s). 629 δ 2.34 (6H, s), 7.39 (1H, t, J = 7.4 Hz), 7.45 (2H, s), 7.52 (1H, 7.4), 7.81 (1H, dd, J = 8.3, 2.7 Hz), 7.88 (1H, dd, J = 8.3, 5.6 Hz), 8.10- 8.16 (2H, m), 10.13 (1H, s), 10.75 (1H, s). 630 δ 2.33 (6H, s), 7.34-7.38 (2H, m), 7.43 (2H, s), 7.51-7.54 (1H, m), 7.58-7.60 (1H, m), 7.67-7.71 (1H, m), 8.00-8.04 (1H, m), 10.10 (1H, s), 10.54 (1H, s). 631 δ 2.34 (6H, s), 7.37 (1H, t, J = 7.9 Hz), 7.45-7.47 (3H, m), 7.52- 7.56 (1H, m), 7.65 (1H, dd, J = 10.2, 2.0 Hz), 7.77 (1H, t, J = 7.9 Hz), 7.99-8.02 (1H, m), 10.11 (1H, s), 10.41 (1H, s). 633 δ 2.34 (6H, s), 7.40 (1H, t, J = 8.1 Hz), 7.45 (2H, s), 7.55 (1H, t, J = 6.5 Hz), 7.92 (1H, d, J = 8.1 Hz), 8.10 (1H, t, J = 6.5 Hz), 8.32 (1H, t, J = 8.1 Hz), 8.43 (1H, s), 10.13 (1H, s), 10.84 (1H, s). 634 δ 2.34 (6H, s), 7.39 (1H, t, J = 8.0 Hz), 7.45 (2H, s), 7.51-7.55 (1H, m), 7.83 (1H, d, J = 8.0 Hz), 7.99 (1H, dd, J = 7.7, 2.2 Hz), 8.12 (1H, t, J = 7.7 Hz), 8.30 (1H, d, J = 2.2 Hz), 10.13 (1H, s), 10.78 (1H, s). 638 δ 2.33 (6H, s), 7.37 (1H, t, J = 8.1 Hz), 7.44 (2H, s), 7.50-7.55 (2H, m), 8.03-8.07 (1H, m), 8.26-8.31 (1H, m), 8.41-8.42 (1H, m), 10.10 (1H, s), 10.54 (1H, s). 639 (CDCl₃) δ 2.38 (6H, s), 7.38 (2H, s), 7.41-7.49 (2H, m), 7.80 (1H, broad-d, J = 11.4 Hz), 7.90-7.94 (1H, m), 8.32-8.35 (1H, m), 8.57- 8.59 (1H, m), 8.62-8.65 (1H, m), 8.74 (1H, s). 648 δ 1.80-1.86 (2H, m), 2.05 (3H, s), 2.33-2.38 (8H, m), 3.99 (2H, t, J = 5.1 Hz), 7.29 (1H, t, J = 7.4 Hz), 7.44-7.48 (3H, m), 7.79 (1H, d, J = 7.4 Hz), 9.25 (1H, s), 10.04 (1H, s). 649 δ 2.29 (6H, s), 7.45 (2H, s), 7.54-7.66 (3H, m), 7.77 (1H, d, J = 8.8 Hz), 7.94 (1H, dd, J = 2.0, 8.1 Hz), 8.00-8.03 (2H, m), 8.19 (1H, d, J = 2.0 Hz), 10.10 (1H, s), 10.29 (1H, s). 650 δ 2.29 (6H, s), 7.45 (2H, s), 7.48-7.65 (4H, m), 7.93-8.02 (3H, m), 8.23 (1H, dd, J = 2.4, 7.3 Hz), 10.03 (1H, s), 10.32 (1H, s). 651 δ 2.29 (6H, s), 7.45 (2H, s), 7.54 (1H, dd, J = 8.8, 9.8 Hz), 7.96- 8.01 (1H, m), 8.23 (2H, d, J = 8.8 Hz), 8.26 (1H, dd, J = 2.4, 8.8 Hz), 8.40 (2H, d, J = 8.8 Hz), 10.05 (1H, s), 10.70 (1H, s). 652 δ 2.29 (6H, s), 7.45 (2H, s), 7.51-7.56 (1H, m), 7.96-8.00 (1H, m), 8.06 (2H, d, J = 8.3 Hz), 8.15 (2H, d, J = 8.3 Hz), 8.25 (1H, dd, J = 2.0, 7.3 Hz), 10.05 (1H, s), 10.61 (1H, s). 653 δ 2.29 (6H, s), 7.33-7.40 (2H, m), 7.45 (2H, s), 7.49-7.54 (1H, m), 7.59-7.65 (1H, m), 7.73-7.77 (1H, m), 7.91-7.95 (1H, m), 8.42 (1H, d, J = 6.3 Hz), 10.05 (1H, s), 10.35 (1H, s). 654 δ 2.29 (6H, s), 7.37-7.45 (4H, m), 7.51 (1H, dd, J = 8.8, 9.8 Hz), 7.93-7.98 (1H, m), 8.06-8.10 (2H, m), 8.22 (1H, dd, J = 2.0, 7.3 Hz), 10.03 (1H, s), 10.37 (1H, s). 655 δ 2.29 (6H, s), 7.45 (2H, s), 7.51-7.56 (1H, m), 7.94-8.00 (3H, m), 8.20 (2H, d, J = 8.3 Hz), 8.25 (1H, dd, J = 2.0, 7.3 Hz), 10.05 (1H, s), 10.59 (1H, s). 656 δ 2.29 (6H, s), 7.23-7.28 (1H, m), 7.42-7.54 (4H, m), 7.80-7.87 (1H, m), 7.91-7.95 (1H, m), 8.41 (1H, d, J = 5.9 Hz), 10.05 (1H, s), 10.36 (1H, s). 657 δ 2.30 (6H, s), 7.46 (2H, s), 7.50-7.59 (2H, m), 7.92-7.96 (1H, m), 8.10 (1H, dd, J = 2.0, 7.3 Hz), 8.52-8.56 (2H, m), 10.07 (1H, s), 10.73 (1H, s). 658 δ 2.31 (6H, s), 7.47 (2H, s), 7.55-7.59 (2H, m), 7.62-7.66 (1H, m), 8.01-8.04 (2H, m), 8.09 (1H, s), 8.54 (1H, s), 8.66 (1H, s), 10.27 (1H, s), 10.79 (1H, s). 659 δ 2.34 (6H, s), 7.40 (1H, t, J = 9.3 Hz), 7.45 (2H, s), 7.53-7.64 (3H, m), 7.97-8.05 (3H, m), 8.14 (1H, dd, J = 2.9, 6.3 Hz), 10.03 (1H, s), 10.48 (1H, s). 660 δ 2.40 (6H, s), 7.45 (2H, s), 7.54-7.65 (4H, m), 7.97-8.03 (3H, m), 8.09 (1H, d, J = 2.4 Hz), 10.20 (1H, s), 10.56 (1H, s). 661 δ 2.41 (6H, s), 7.45 (2H, s), 7.54-7.65 (3H, m), 7.72 (1H, d, J = 8.8 Hz), 7.94-7.99 (3H, m), 8.08 (1H, d, J = 2.9 Hz), 10.20 (1H, s), 10.56 (1H, s). 662 δ 2.44 (6H, s), 7.45 (2H, s), 7.53-7.65 (3H, m), 7.79 (1H, dd, J = 2.4, 8.3 Hz), 7.90-7.98 (3H, m), 8.05 (1H, d, J = 2.4 Hz), 10.15 (1H, s), 10.53 (1H, s). 663 δ 2.35 (6H, s), 7.32 (1H, t, J = 8.3), 7.46 (2H, s), 7.54-7.77 (4H, m), 8.00 (2H, dd, J = 1.5, J = 8.3), 10.3 (1H, s), 10.6 (1H, s). 664 (CDCl₃) δ 2.53 (6H, s), 7.35 (2H, s), 7.52-7.63 (5H, m), 7.92 (2H, d, J = 8.8 Hz), 8.46 (1H, d, J = 8.8 Hz), 8.57 (1H, s). 665 δ 2.34 (6H, s), 7.37 (1H, t, J = 7.8 Hz), 7.44 (2H, s), 7.53-7.65 (4H, m), 7.77-7.81 (1H, m), 7.99-8.02 (2H, m), 10.09 (1H, broad), 10.29 (1H, broad). 668 δ 2.34 (6H, s), 7.33-7.40 (3H, m), 7.44 (2H, s), 7.51-7.56 (1H, m), 7.58-7.65 (1H, m), 7.72-7.77 (1H, m), 8.00 (1H, t, J = 8.3 Hz), 10.10 (1H, s), 10.34 (1H, s). 670 δ 2.28 (6H, s), 7.31-7.44 (5H, m), 7.57 (1H, t, J = 6.3 Hz), 7.79 (1H, t, J = 7.3 Hz), 8.07-8.09 (2H, m), 10.09 (1H, s), 10.32 (1H, s). 676 δ 7.34 (6H, s), 7.39 (1H, t, J = 7.2 Hz), 7.44 (2H, s), 7.59 (1H, t, J = 7.2 Hz), 7.83 (1H, t, J = 7.2 Hz), 7.99 (2H, d, J = 8.8 Hz), 8.15 (2H, d, J = 8.8 Hz), 10.1 (1H, s), 10.57 (1H, s). 679 δ 2.35 (6H, s), 7.4 (1H, t, J = 7.3 Hz), 7.44 (2H, s), 7.61 (1H, t, J = 7.3 Hz), 7.84 (1H, t, J = 7.3 Hz), 8.24 (2H, d, J = 8.8 Hz), 8.41 (2H, d, J = 8.8 Hz), 10.11 (1H, s), 10.66 (1H, s). 682 δ 2.35 (6H, s), 7.38 (1H, t, J = 8.1 Hz), 7.44 (2H, s), 7.49 (1H, d, J = 8.1 Hz), 7.56 (1H, d, J = 8.1 Hz), 8.07 (2H, d, J = 8.8 Hz), 8.14 (2H, d, J = 8.8 Hz), 10.1 (1H, s), 10.43 (1H, s). 686 δ 2.34 (6H, s), 7.23-7.28 (2H, m), 7.38 (1H, t, J = 7.8 Hz), 7.44 (2H, s), 7.52-7.65 (2H, m), 8.05-8.10 (1H, m), 10.12 (1H, s), 10.88 (1H, s). 699 δ 2.34 (6H, s), 3.39 (3H, s), 7.39 (1H, t, J = 7.8 Hz), 7.44 (2H, s), 7.49-7.59 (2H, m), 8.08-8.13 (2H, m), 8.55 (1H, dd, J = 4.9, 2.0 Hz), 10.12 (1H, s), 10.73 (1H, s). 708 (CDCl₃) δ 7.39 (1H, t, J = 7.8 Hz), 7.48-7.64 (3H, m), 7.88-7.96 (4H, m), 8.09-8.13 (2H, m), 8.69 (1H, t, J = 7.8 Hz), 8.75 (1H, d, J = 7.8 Hz). 711 (CDCl₃) δ 7.22 (1H, d, J = 8.3 Hz), 7.35-7.40 (2H, m), 7.56-7.62 (1H, m), 7.91 (1H, t, J = 7.3 Hz), 7.96 (2H, s), 8.15 (1H, d, J = 13.3 Hz), 8.22 (1H, dt, J = 1.9, 8.3 Hz), 8.73 (1H, dt, J = 1.5, 8.3 Hz), 8.92 (1H, d, J = 17.1 Hz). 719 (CDCl₃) δ 7.41 (1H, t, J = 8.3 Hz), 7.85 (2H, d, J = 8.3 Hz), 7.92 (1H, d, J = 6.9 Hz), 7.96 (2H, s), 8.03 (2H, d, J = 8.3 Hz), 8.06 (1H, s), 8.10 (1H, s), 8.63 (1H, dt, J = 1.5, 8.3 Hz). 722 (CDCl₃) δ 7.42 (1H, t, J = 8.3 Hz), 7.93 (1H, d, J = 5.3 Hz), 7.96 (2H, s), 8.06 (1H, d, J = 12.2 Hz), 8.10 (2H, d, J = 8.8 Hz), 8.13 (1H, s), 8.40 (2H, d, J = 8.8 Hz), 8.64 (1H, dt, J = 1.5, 8.3 Hz). 791 (CDCl₃) δ 2.34 (6H, s), 7.37 (1H, t, J = 7.8 Hz), 7.45 (2H, s), 7.54 (2H, t, J = 7.8 Hz), 7.61 (1H, d, J = 7.8 Hz), 7.80 (1H, d, J = 11.7 Hz), 7.82-7.87 (1H, m), 7.92 (2H, d, J = 7.8 Hz), 8.12 (1H, s), 8.62 (1H, dt, J = 2.0, 7.8 Hz). 831 (CDCl₃) δ 7.46-7.64 (6H, m), 7.93-7.96 (4H, m), 8.61 (1H, s), 7.75 (1H, dd, J = 1.9, 8.3 Hz). 832 (CDCl₃) δ 7.24 (1H, d, J = 8.3 Hz), 7.36 (1H, t, J = 8.3 Hz), 7.47 (1H, t, J = 8.3 Hz), 7.55-7.62 (3H, m), 7.96 (2H, s), 8.21 (1H, dt, J = 2.0, 8.3 Hz), 8.77 (1H, dd, J = 2.0, 8.3 Hz), 9.33 (1H, d, J = 16.6 Hz). 833 (CDCl₃) δ 7.45-7.52 (3H, m), 7.60 (1H, d, J = 8.8 Hz), 7.96 (2H, s), 8.29 (1H, d, J = 7.8 Hz), 8.57 (1H, dd, J = 2.0, 4.4 Hz), 8.72 (1H, d, J = 7.8 Hz), 9.00 (1H, s). 1001 δ 2.20 (6H, s), 3.45 (3H, s), 7.23-7.30 (5H, m), 7.43-7.45 (4H, m), 7.73-7.76 (2H, m), 9.88 (1H, s). 1013 δ 2.20 (6H, s), 3.48 (3H, s), 7.39-7.97 (8H, m), 7.43 (2H, s), 9.90 (1H, s). 1016 δ 2.21 (6H, s), 3.46 (3H, s), 7.40-8.03 (10H, m), 9.91 (1H, s). 1032 δ 2.08 (3H, s), 2.30 (6H, s), 7.45 (2H, s), 7.47 (1H, d, J = 7.8 Hz), 7.54 (1H, t, J = 7.8 Hz), 7.66 (1H, d, J = 7.8 Hz), 7.75 (1H, d, J = 7.8 Hz), 7.82 (1H, d, J = 7.8 Hz), 8.04 (1H, dd, J = 2.0, 7.8 Hz), 8.13 (1H, s), 8.35 (1H, s), 9.99 (1H, s), 10.16 (1H, s), 10.48 (1H, s). 1043 (CDCl₃) δ 1.38 (6H, m), 2.37 (6H, s), 3.13 (1H, broad), 3.33 (3H, broad), 3.78 (1H, broad), 3.89 (1H, broad), 7.37 (2H, s), 7.48 (1H, d, J = 7.8 Hz), 7.58 (1H, t, J = 7.8 Hz), 7.77 (1H, s), 7.90 (1H, s), 7.93 (1H, broad). 1089 (CDCl₃) δ 0.89 (3H, t, J = 7.3 Hz), 1.53-1.62 (2H, m), 2.61 (2H, t, J = 7.3 Hz), 3.50 (3H, broad), 6.80 (1H, broad), 7.03 (1H, broad), 7.22 (1H, broad), 7.34 (3H, broad), 7.47 (1H, s), 7.67-7.76 (3H, broad-m), 7.93 (1H, s). 1091 (CDCl₃) δ 0.88 (3H, t, J = 7.3 Hz), 1.53-1.63 (2H, m), 2.62 (2H, t, J = 7.8 Hz), 3.52 (3H, s), 6.83-6.89 (2H, m), 7.26-7.32 (3H, m), 7.41 (1H, t, J = 7.8 Hz), 7.48 (1H, s), 7.66 (1H, s), 7.76 (2H, d, J = 8.8 Hz), 7.93 (1H, d, J = 1.5 Hz). 1097 (CDCl₃) δ 0.90 (3H, t, J = 7.3 Hz), 1.55-1.65 (2H, m), 2.64 (2H, t, J = 7.8 Hz), 3.55 (3H, s), 7.27 (1H, s), 7.40-7.44 (3H, m), 7.49-7.51 (3H, m), 7.59 (1H, s), 7.69 (1H, s), 7.76 (1H, d, J = 7.8 Hz), 7.95 (1H, s). 1100 (CDCl₃) δ 0.88 (3H, t, J = 7.3 Hz), 1.54-1.64 (2H, m), 2.63 (2H, t, J = 7.8 Hz), 3.56 (3H, s), 7.29 (1H, s), 7.40-7.50 (4H, m), 7.59 (1H, s), 7.71 (1H, s), 7.76 (1H, d, J = 7.3 Hz), 7.94 (1H, d, J = 1.5 Hz), 8.06 (2H, d, J = 8.8 Hz). 1125 (CDCl₃) δ 2.25 (6H, s), 3.54 (3H, s), 6.84 (1H, broad-s), 7.00-7.10 (2H, m), 7.20-7.40 (6H, m), 7.50-7.60 (1H, broad), 7.60-7.70 (1H, broad). 1126 (CDCl₃) δ 3.57 (3H, s), 7.20-7.24 (2H, m), 7.29-7.32 (3H, m), 7.34 (1H, t, J = 7.8 Hz), 7.40-7.44 (2H, m), 7.57 (1H, d, J = 7.8 Hz), 7.86-7.91 (1H, m), 7.92 (2H, s). 1206 δ 1.17 (3H, broad), 2.22 (6H, s), 3.94 (2H, broad), 7.01-7.08 (2H, m), 7.29-7.43 (6H, m), 7.72-7.77 (2H, m), 9.90 (1H, s). 1207 δ 1.26 (3H, t, J = 6.8 Hz), 2.04 (6H, s), 4.11 (2H, q, J = 6.8 Hz), 7.16-7.70 (12H, m). 1208 δ 2.28 (6H, s), 3.36 (3H, s), 7.27-7.32 (6H, m), 7.43 (2H, s), 7.55- 7.57 (2H, broad), 9.96 (1H, s). 1209 δ 2.28 (6H, s), 3.47 (3H, s), 6.98 (1H, broad), 7.11 (2H, broad), 7.19 (1H, broad), 7.37 (1H, broad), 7.44 (2H, s), 7.51 (1H, broad), 7.74 (1H, broad), 9.94 (1H, s). 1210 δ 2.23 (3H, s), 2.29 (6H, s), 7.07-7.26 (5H, m), 7.44 (2H, s), 7.56- 7.77 (2H, m), 9.98 (1H, s). 1211 δ 2.24 (3H, s), 2.28 (6H, s), 7.08-7.09 (2H, m), 7.22-7.28 (2H, m), 7.44 (2H, s), 7.51-7.58 (3H, m), 9.99 (1H, s). 1212 δ 2.29 (6H, s), 3.12 (3H, s), 7.17-8.02 (9H, m), 9.95 (1H, s). 1213 δ 2.26 (6H, s), 3.41 (3H, s), 7.12-8.34 (9H, m), 9.92 (1H, s). 1214 δ 2.26 (6H, s), 3.40 (3H, s), 7.29 (1H, broad), 7.44 (2H, s), 7.59- 7.81 (4H, m), 8.12 (2H, broad), 9.91 (1H, s). 1215 δ 2.26 (6H, s), 3.40 (3H, s), 7.31-7.39 (7H, m), 7.50-7.56 (1H, m), 7.81-7.83 (1H, m), 9.94 (1H, s). 1216 δ 2.27 (6H, s), 3.39 (3H, s), 7.31 (1H, m), 7.47 (2H, s), 7.60-7.67 (3H, m), 7.72-7.80 (3H, m), 9.96 (1H, s). 1217 δ 2.27 (6H, s), 3.37 (3H, s), 7.29 (2H, broad), 7.44-7.48 (3H, m), 7.59-7.64 (2H, m), 7.76 (2H, broad), 9.94 (1H, s). 1218 δ 2.27 (6H, s), 3.39 (3H, s), 7.03-7.72 (9H, m), 9.94 (1H, s). 1219 δ 2.28 (6H, s), 3.36 (3H, s), 7.18-8.04 (9H, m), 9.98 (1H, m). 1220 δ 2.28 (6H, s), 3.34 (3H, s), 7.12-7.56 (9H, m), 9.97 (1H, s). 1229 δ 2.28 (6H, s), 3.39 (3H, s), 7.02-7.28 (2H, m), 7.35-7.43 (2H, m), 7.55-7.70 (2H, m), 7.93-7.99 (2H, m), 9.95 (1H, m). 1235 δ 2.26 (6H, s), 3.43 (3H, s), 7.27 (1H, t, J = 7.8 Hz), 7.44 (2H, s), 7.58-7.65 (2H, m), 7.71 (1H, t, J = 7.8), 8.00 (1H, dd, J = 8.3, 2.0 Hz), 8.04 (1H, dd, J = 9.3, 2.0 Hz), 9.91 (1H, s). 1236 δ 2.29 (6H, s), 3.41 (3H, s), 7.44-7.46 (3H, m), 7.59-7.61 (2H, m), 7.72-7.77 (1H, m), 7.88 (1H, d, J = 6.8 Hz), 7.95-7.99 (1H, m), 9.95 (1H, s). 1237 δ 2.29 (6H, s), 3.40 (3H, s), 7.08-7.91 (8H, m), 9.94 (1H, s). 1238 δ 2.28 (6H, s), 3.39 (3H, s), 7.21-7.28 (1H, m), 7.34-7.44 (3H, m), 7.54-7.60 (2H, m), 7.79-7.91 (2H, m), 9.95 (1H, m). 1245 δ 2.28 (6H, s), 3.41 (3H, s), 7.25 (1H, t, J = 7.6 Hz), 7.36 (1H, d, J = 4.7 Hz), 7.44 (2H, s), 7.57-7.64 (2H, m), 7.92 (1H, d, J = 7.6 Hz), 8.32 (1H, dd, J = 4.7, 1.9 Hz), 9.97 (1H, s). 1246 δ 2.31 (6H, s), 3.60 (3H, s), 7.25-7.31 (2H, m), 7.44 (2H, s), 7.57- 7.59 (2H, m), 7.97-8.01 (1H, m), 8.17-8.18 (1H, m), 9.97 (1H, s). 1247 δ 2.28 (6H, s), 3.39 (3H, s), 7.33 (1H, d, J = 7.6 Hz), 7.44 (2H, s), 7.61-7.69 (3H, m), 7.80 (1H, broad), 8.30 (1H, broad), 10.01 (1H, s). 1255 δ 2.29 (6H, s), 3.35 (3H, s), 7.19-7.70 (10H, m), 9.98 (1H, s). 1256 δ 2.28 (6H, s), 2.30 (3H, s), 3.32 (3H, s), 6.98-7.72 (9H, m), 9.93 (1H, s). 1257 δ 2.23 (3H, s), 2.29 (6H, s), 3.34 (3H, s), 7.07-7.38 (5H, m), 7.53- 7.76 (2H, m), 7.43 (2H, s), 9.98 (1H,s). 1258 δ 2.27 (6H, s), 2.33 (3H, s), 3.31 (3H, s), 6.98-7.51 (9H, s), 9.93 (1H, s). 1259 δ 2.29 (6H, s), 3.41 (3H, s), 7.18 (1H, J = 7.3 Hz), 7.44 (2H, s), 7.46-7.57 (2H, m), 7.67 (1H, t, J = 7.3 Hz), 7.73-7.82 (2H, m), 8.01 (1H, d, J = 7.8 Hz), 9.95 (1H, s). 1260 δ 2.26 (6H, s), 3.36 (3H, s), 7.42 (2H, s), 7.59 (1H, broad), 7.7 (1H, broad), 7.82 (1H, t, J = 7.9 Hz), 8.2 (1H, broad), 8.34-8.37 (1H, m), 8.48 (1H, dd, J = 7.9, 1.7 Hz), 8.62 (1H, t, J = 2.0 Hz), 9.92 (1H, s). 1261 δ 2.27 (6H, s), 3.37 (3H, s), 7.43 (2H, s), 7.59-7.65 (2H, m), 8.11 (1H, broad), 8.18 (2H, d, J = 8.8 Hz), 8.29 (2H, d, J = 8.8 Hz), 9.91 (1H, s). 1262 δ 2.33 (6H, s), 3.35 (3H, s), 7.30-7.83 (9H, m), 9.93 (1H, s). 1263 δ 2.27 (6H, s), 3.37 (3H, s), 7.18-7.80 (9H, m), 9.96 (1H, s). 1264 δ 2.27 (6H, s), 3.35 (3H, s), 7.43 (2H, s), 7.48 (1H, broad), 7.58 (1H, broad), 7.75 (1H, broad), 7.99 (2H, d, J = 8.5 Hz), 8.08 (2H, d, J = 8.5 Hz), 9.95 (1H, s). 1265 δ 2.27 (6H, s), 3.36 (3H, s), 7.03-7.73 (9H, m), 9.93 (1H, s). 1266 δ 2.28 (6H, s), 3.35 (2H, s), 7.18-7.61 (9H, m), 9.99 (1H, s). 1267 δ 2.28 (6H, s), 3.39 (3H, s), 7.11-7.18 (3H, m), 7.26-7.30 (1H, t, J = 7.8 Hz), 7.40-7.47 (3H, m), 7.58 (2H, t, J = 7.6 Hz), 9.96 (1H, s). 1274 δ 2.27 (6H, s), 3.37 (3H, s), 7.29 (3H, broad), 7.41-7.47 (4H, m), 7.59-7.61 (2H, m), 9.95 (1H, s). 1293 δ 2.28 (6H, s), 3.41 (3H, s), 7.25 (1H, t, J = 7.6 Hz), 7.35 (1H, dd, J = 7.3, 4.9 Hz), 7.43 (2H, s), 7.57-7.63 (2H, m), 7.91 (1H, d, J = 7.6 Hz), 8.32 (1H, dd, J = 4.9, 2.0 Hz), 9.96 (1H, s). 1294 δ 2.28 (6H, s), 3.39 (3H, s), 7.31-7.35 (1H, m), 7.42 (2H, s), 7.43- 7.48 (1H, m), 7.61-7.75 (2H, m), 7.80 (1H, s), 8.32 (1H, broad), 10.01 (1H, s). 1463 δ 2.25 (6H, s), 3.38 (3H, s), 7.27-7.41 (6H, m), 7.45 (2H, s), 7.90 (1H, broad), 8.05 (1H, d, J = 6.8 Hz), 9.96 (1H, s). 1464 δ 2.23 (6H, s), 3.42 (3H, s), 7.41 (1H, broad), 7.45 (2H, s), 7.60 (2H, broad), 7.90 (1H, broad), 8.08-8.13 (3H, broad), 9.93 (1H, s). 1465 δ 2.25 (6H, s), 3.40 (3H, s), 7.39-7.42 (1H, m), 7.45 (2H, s), 7.50 (1H, broad), 7.78 (1H, broad), 7.91 (1H, broad), 7.97-8.10 (3H, m), 9.94 (1H, s). 1478 δ 2.29 (6H, s), 3.24 (3H, s), 6.84 (1H, d, J = 7.8 Hz), 7.12 (1H, t, J = 7.8 Hz), 7.33 (2H, s), 7.50-7.64 (4H, m), 7.85-7.88 (2H, m), 7.98-8.03 (1H, m), 10.22 (1H, s). 1479 δ 2.41 (3H, s), 3.25 (3H, s), 6.95 (1H, dd, J = 1.5, 7.8 Hz), 7.16 (1H, t, J = 7.8 Hz), 7.50-7.64 (4H, m), 7.68 (1H, s), 7.86-7.88 (2H, m), 7.93 (1H, t, J = 1.5 Hz), 7.98-8.00 (1H, m), 10.24 (1H, s). 1480 (CDCl₃) δ 3.34 (3H, s), 7.13-7.19 (2H, m), 7.49-7.58 (3H, m), 7.70- 7.73 (2H, m), 7.78-7.91 (4H, m), 8.12 (1H, s). 1481 (CDCl₃) δ 3.35 (3H, s), 7.15-7.20 (3H, m), 7.32 (1H, t, J = 7.8 Hz), 7.51-7.55 (1H, m), 7.71 (1H, d, J = 2.9 Hz), 7.72 (1H, d, J = 2.0 Hz), 7.80 (2H, s), 8.14 (1H, dt, J = 2.0, 7.8 Hz), 8.37 (1H, d, J = 16.1 Hz). 1482 δ 1.18 (3H, t, J = 7.3 Hz), 2.30 (6H, s), 3.76 (2H, q, J = 7.3 Hz), 6.81 (1H, d, J = 7.8 Hz), 7.11 (1H, t, J = 7.8 Hz), 7.33 (2H, s), 7.50- 7.62 (4H, m), 7.84-7.88 (2H, m), 7.95-8.00 (1H, m), 10.20 (1H, s). 1483 δ 1.44 (6H, d, J = 6.3 Hz), 2.07 (6H, s), 5.35 (1H, septet, J = 6.3 Hz), 6.84 (1H, d, J = 7.8 Hz), 7.21 (1H, t, J = 7.8 Hz), 7.21 (2H, s), 7.50-7.61 (3H, m), 7.75 (1H, dd, J = 1.5, 7.8 Hz), 7.86-7.89 (3H, m), 10.29 (1H, s). 1484 δ 2.18 (3H, s), 2.32 (6H, s), 7.37-7.59 (11H, m), 10.42 (1H, s). 1485 δ 2.34 (3H, s), 2.35 (6H, s), 7.34-8.02 (10H, m), 10.33 (1H, s). 1486 δ 2.33 (3H, s), 2.36 (6H, s), 7.29-8.12 (9H, m), 10.37 (1H, s). 1487 δ 2.20 (6H, s), 3.08 (3H, s), 3.20 (3H, s), 6.93-7.39 (10H, m), 7.45- 7.51 (1H, m). 1607 (CDCl₃) δ 3.31 (3H, s), 3.35 (3H, s), 6.81 (1H, dt, J = 6.8, 1.0 Hz), 6.94 (1H, t, J = 7.8 Hz), 7.10-7.24 (5H, m), 7.35-7.40 (1H, m), 7.41 (1H, s), 7.78 (2H, s). 1617 (CDCl₃) δ 3.30 (3H, s), 3.33 (3H, s), 6.76-7.00 (4H, m), 7.19-7.23 (3H, m), 7.37 (1H, s), 7.77 (2H, s). 1645 (CDCl₃) δ 3.30 (3H, s), 3.36 (3H, s), 6.96-7.06 (3H, m), 7.12-7.16 (1H, m), 7.39-7.42 (2H, m), 7.95 (2H, s), 8.24 (1H, s). 1654 (CDCl₃) δ 3.30 (3H, s), 3.42 (3H, s), 7.01 (1H, d, J = 7.3 Hz), 7.10 (1H, t, J = 7.8 Hz), 7.16 (1H, dd, J = 1.4, 7.8 Hz), 7.41 (1H, t, J = 1.4 Hz), 7.54 (1H, dd, J = 1.9 Hz), 7.56 (1H, d, J = 1.9 Hz), 7.80 (1H, s), 7.81 (2H, s). 1655 (CDCl₃) δ 3.29 (3H, s), 3.38 (3H, s), 3.78 (3H, s), 6.73 (1H, d, J = 8.3 Hz), 6.96 (1H, d, J = 8.3 Hz), 7.04 (1H, t, J = 7.8 Hz), 7.08 (1H, d, J = 1.5 Hz), 7.14 (1H, d, J = 7.8 Hz), 7.40 (1H, s), 7.54 (1H, d, J = 8.3 Hz), 7.81 (2H, s). 1697 δ 2.23 (6H, s), 3.32 (3H, s), 3.39 (3H, s), 7.15-7.43 (10H, m). 2001 (CDCl₃) δ 2.36 (6H, s), 7.36 (2H, s), 7.53-7.57 (2H, m), 7.61-7.65 (1H, m), 7.95-8.03 (3H, m), 8.08 (1H, dd, J = 7.3, 1.0 Hz), 8.52 (1H, broad-s), 8.62 (1H, dd, J = 8.3, 1.0 Hz), 9.19 (1H, broad-s). 2004 δ 2.30 (6H, s), 7.37-7.43 (2H, m), 7.46 (2H, s), 7.65 (1H, d, J = 8.1 Hz), 7.83 (1H, dd, J = 7.5, 5.6 Hz), 7.88 (1H, d, J = 7.5 Hz), 8.13 (1H, t, J = 8.1 Hz), 8.40 (1H, d, J = 8.1 Hz), 10.08 (1H, s), 10.62 (1H, s). 2032 δ 2.30 (6H, s), 7.46 (2H, s), 7.75-7.78 (1H, m), 7.91 (1H, dd, J = 7.3, 1.0 Hz), 8.13-8.18 (2H, m), 8.27 (1H, d, J = 8.0 Hz), 8.56 (1H, d, J = 8.0 Hz), 8.77 (1H, d, J = 1.0 Hz), 10.62 (1H, s), 10.75 (1H, s). 2033 δ 2.27 (6H, s), 6.16 (2H, s), 6.71 (1H, d, J = 7.6 Hz), 7.01 (2H, d, J = 1.0 Hz), 7.24 (1H, d, J = 6.9 Hz), 7.42 (2H, s), 7.59 (1H, dd, J = 7.6, 6.9 Hz), 7.65 (1H, s), 9.94 (1H, s). 2034 δ 2.32 (6H, s), 7.47 (2H, s), 7.90-7.93 (3H, m), 8.15 (1H, t, J = 8.0 Hz), 8.37 (1H, d, J = 8.0 Hz), 8.83 (2H, dd, J = 4.6, 1.7 Hz), 10.12 (1H, s), 10.92 (1H, s). 2035 δ 2.30 (6H, s), 7.46 (2H, s), 7.55-7.56 (1H, m), 7.89 (1H, d, J = 7.4 Hz), 8.14 (1H, t, J = 7.8 Hz), 8.34-8.41 (2H, m), 8.45 (1H, dd, J = 5.4, 1.2 Hz), 10.03 (1H, s), 10.90 (1H, s). 2036 δ 2.29 (6H, s), 7.45 (2H, s), 7.59 (1H, t, J = 6.3 Hz), 7.88 (1H, d, J = 6.3 Hz), 8.12-8.16 (2H, m), 8.39 (1H, m), 8.55 (1H, m), 9.93 (1H, s), 11.25 (1H, s). 2037 δ 2.32 (6H, s), 7.47 (2H, s), 7.67 (1H, d, J = 7.6 Hz), 7.75 (1H, d, J = 8.3 Hz), 7.90 (1H, d, J = 7.6 Hz), 8.14 (1H, t, J = 7.6 Hz), 8.29 (1H, dd, J = 8.3 Hz, 2.0 Hz), 8.89 (1H, d, J = 2.0 Hz), 10.07 (1H, s), 10.97 (1H, s). 2082 δ 2.20 (6H, s), 3.58 (3H, s), 7.29-7.39 (5H, m), 7.43 (2H, s), 7.50 (1H, d, J = 7.4 Hz), 7.83 (1H, t, J = 7.4 Hz), 7.94 (1H, t, J = 7.4 Hz), 9.91 (1H, s). 2085 δ 2.22 (6H, s), 3.57 (3H, s), 7.12 (1H, t, J = 9.2 Hz), 7.20 (1H, t, J = 7.3 Hz), 7.28-7.30 (1H, m), 7.44 (2H, s), 7.55 (1H, t, J = 7.2 Hz), 7.63 (1H, broad), 7.87 (1H, d, J = 7.2 Hz), 7.98 (1H, t, J = 7.2 Hz), 9.90 (1H, s). 2093 δ 2.14 (6H, s), 3.57 (3H, s), 7.42 (2H, s), 7.66-7.87 (3H, m), 7.96- 8.09 (4H, m), 9.77 (1H, s). 2116 δ 2.23 (6H, s), 3.55 (3H, s), 7.45 (3H, s), 7.89-9.91 (2H, m), 8.03- 8.10 (3H, m), 9.82 (1H, s). 2117 δ 2.13 (6H, s), 3.58 (3H, s), 7.42 (2H, s), 7.46 (1H, d, J = 8.2 Hz), 7.72-7.75 (2H, m), 7.90 (1H, d, J = 8.2 Hz), 8.08 (1H, t, J = 8.2 Hz), 8.35 (1H, d, J = 2.0 Hz), 9.83 (1H, s). 2162 (CDCl₃) δ 2.38 (6H, s), 7.38 (2H, s), 7.53-7.57 (2H, m), 7.62 (1H, d, J = 7.8 Hz), 7.68 (1H, dd, J = 4.9, 1.5 Hz), 7.85 (1H, broad-s), 7.95 (2H, d, J = 7.8 Hz), 8.52 (1H, d, J = 4.9 Hz), 8.22 (1H, broad- s), 8.88 (1H, s). 2163 (CDCl₃) δ 2.36 (6H, s), 7.38 (2H, s), 7.55-7.59 (2H, m), 7.64-7.72 (2H, m), 7.75 (1H, broad-s), 8.01 (2H, d, J = 7.3 Hz), 8.41 (1H, d, J = 6.8 Hz), 9.14 (1H, d, J = 2.4 Hz), 10.9 (1H, broad-s). 2164 (CDCl₃) δ 2.34 (6H, s), 7.47 (2H, s), 7.62-7.65 (2H, m), 7.70-7.81 (2H, m), 8.04-8.04 (3H, m), 8.64 (1H, dd, J = 8.3, 1.5 Hz), 10.9 (1H, broad-s), 12.3 (1H, broad-s). 2165 δ 2.35 (6H, s), 7.29-8.03 (10H, m), 8.75 (1H, d, J = 2.0 Hz). 2168 δ 2.25 (6H, s), 3.32 (3H, s), 7.26 (1H, d, J = 7.7 Hz), 7.38 (1H, d, J = 7.7 Hz), 7.44 (2H, s), 7.55 (1H, t, J = 7.7 Hz), 7.90 (3H, m), 8.11 (2H, m), 12.40 (1H, s). 2201 (CDCl₃) δ 2.38 (6H, s), 7.25-8.00 (1H, m), 8.34 (1H, s), 8.85 (1H, broad.). 2202 (CDCl₃) δ 2.36 (6H, s), 7.37 (2H, s), 7.47-7.61 (5H, m), 7.85-8.03 (4H, m), 8.57 (1H, s), 9.18 (1H, s). 2203 (CDCl₃) δ 2.38 (6H, s), 7.41 (2H, s), 7.45-7.55 (4H, m), 7.90-7.96 (4H, m), 8.57 (1H, broad), 8.74 (1H, broad), 9.18 (1H, broad). ¹H-NMR (CDCl₃, ppm) I-1 δ 2.34 (6H, s), 3.87 (2H, broad-s), 6.86-6.89 (1H, m), 7.21-7.30 (3H, m), 7.33 (2H, s), 7.39 (1H, s) I-2 δ 2.34 (6H, s), 3.87 (2H, broad), 6.86-6.89 (1H, m), 7.20-7.35 (6H, m) I-4 δ 2.60 (3H, s), 3.92 (2H, broad-s), 6.89-6.92 (1H, m), 7.24-7.32 (3H, m), 7.46 (1H, s), 7.76 (1H, broad-s) I-5 δ 2.27 (6H, s), 3.31 (3H, s), 6.40-6.43 (1H, m), 6.54-6.58 (1H, m), 6.71 (1H, t, J = 2.0 Hz), 6.76-6.86 (1H, m), 7.22 (2H, s) I-6 δ 1.45 (6H, d, J = 6.3 Hz), 2.07 (6H, s), 3.53 (2H, broad), 5.37 (1H, septet, J = 6.3 Hz), 6.56-6.63 (3H, m), 6.96 (1H, t, J = 7.8 Hz), 7.16 (2H, s) I-7 δ 1.17 (3H, t, J = 7.6 Hz), 2.28 (3H, s), 2.65 (2H, q, J = 7.6 Hz), 3.85 (2H, broad-s), 6.82-6.85 (1H, m), 7.21-7.23 (3H, m), 7.34 (2H, s), 7.64 (1H, s) I-8 δ 1.22 (6H, t, J = 7.6 Hz), 2.69 (4H, q, J = 7.6 Hz), 3.86 (2H, broad- s), 6.86-6.89 (1H, m), 7.15-7.36 (4H, m), 7.38 (2H, s) I-9 δ 1.23 (3H, t, J = 7.3 Hz), 2.76 (2H, q, J = 7.3 Hz), 3.88 (2H, broad- s), 6.88-6.91 (1H, m), 7.26-7.32 (3H, m), 7.50 (1H, s), 7.53 (1H, s), 7.95 (1H, d, J = 1.5 Hz) I-10 δ 1.22 (6H, d, J = 6.8 Hz), 2.32 (3H, s), 3.17 (1H, septet, J = 6.8 Hz), 3.87 (2H, broad-s), 6.85-6.93 (1H, m), 7.20-7.29 (3H, m), 7.35 (1H, s), 7.40-7.45 (2H, m). I-11 δ 2.35 (3H, s), 3.85 (5H, s), 6.85-6.89 (1H, m), 6.95 (1H, s), 7.13 (1H, s), 7.23-7.30 (3H, m), 7.62 (1H, s) I-12 δ 1.25 (3H, t, J = 7.6 Hz), 2.76 (2H, q, J = 7.6 Hz), 3.88 (2H, broad- s), 6.87-6.91 (1H, m), 7.24-7.31 (3H, m), 7.47 (1H, s), 7.55 (1H, s), 7.57 (1H, s) I-13 δ 2.35 (3H, s), 2.57 (3H, d, J = 6.8 Hz), 3.88 (2H, broad-s), 6.88- 6.91 (1H, m), 7.25-7.34 (4H, m), 7.67 (1H, s) I-14 δ 2.41 (3H, s), 3.88 (2H, broad-s), 6.87-6.91 (1H, m), 7.25-7.31 (3H, m), 7.47 (1H, s), 7.65 (1H, s), 7.72 (1H, s) I-15 δ 1.23 (3H, t, J = 7.3 Hz), 2.74 (2H, q, J = 7.3 Hz), 3.87 (2H, broad- s), 6.86-6.91 (1H, m), 7.25-7.31 (3H, m), 7.50 (1H, s), 7.59 (1H, s), 7.73 (1H, d, J = 1.5 Hz) I-16 (DMSO-d₆) δ 0.84 (3H, t, J = 7.3 Hz), 1.48-1.58 (2H, m), 2.66 (2H, t, J = 7.3 Hz), 5.36 (2H, broad-s), 6.77 (1H, dd, J = 1.0 Hz, 7.8 Hz), 7.10-7.19 (3H, m), 7.59 (1H, s), 7.80 (1H, s), 10.03 (1H, s) I-17 δ 0.90 (3H, t, J = 7.3 Hz), 1.25-1.37 (2H, m), 1.55-1.63 (2H, m), 2.72 (2H, t, J = 7.8 Hz), 3.89 (2H, broad), 6.87-6.91 (1H, m), 7.24- 7.31 (3H, m), 7.48 (1H, s), 7.55 (1H, s), 7.73 (1H, d, J = 1.5 Hz) I-18 δ 2.39 (3H, s), 2.66 (3H, d, J = 6.9 Hz), 7.43 (1H, s), 7.75-7.79 (2H, m), 8.33 (1H, d, J = 8.3 Hz), 8.48 (1H, d, J = 8.3 Hz), 8.80 (1H, s) I-19 δ 2.41 (3H, s), 3.88 (2H, s), 6.86-6.91 (1H, m), 7.28-7.32 (3H, m), 7.49 (1H, s), 7.58 (1H, s), 7.93 (1H, d, J = 1.2 Hz) I-20 δ 0.91 (3H, t, J = 7.3 Hz), 1.58-1.67 (2H, m), 2.69 (2H, t, J = 7.8 Hz), 3.88 (2H, broad-s), 6.87-6.90 (1H, m), 7.26-7.31 (3H, m), 7.50 (1H, s), 7.54 (1H, s), 7.95 (1H, d, J = 2.0 Hz) I-21 δ 2.33 (6H, s), 3.87 (2H, broad-s), 6.86-6.89 (1H, m), 7.21-7.29 (3H, m), 7.34 (2H, s), 7.52 (1H, s) I-22 δ 2.32 (6H, s), 3.86 (2H, broad-s), 6.85-6.88 (1H, m), 7.20-7.28 (3H, m), 7.33 (2H, s), 7.60 (1H, s) I-23 δ 3.99 (2H, broad-s), 6.85-6.88 (1H, m), 7.23-7.34 (3H, m), 7.91 (2H, s), 8.69 (1H, s) I-24 (DMSO-d₆) δ 5.39 (2H, broad-s), 6.77-6.80 (1H, m), 7.12-7.19 (3H, m), 8.49 (2H, s), 10.53 (1H, s) I-26 δ 3.88 (2H, s), 6.90 (1H, d, J = 6.8 Hz), 7.23-7.32 (3H, m), 7.60 (1H, s), 7.92 (2H, s) I-27 δ 3.89 (2H, broad-s), 6.90 (1H, dt, J = 2.5 Hz, 6.3 Hz), 7.25-7.32 (3H, m), 7.59 (1H, s), 7.72 (2H, s) I-28 δ 3.89 (2H, broad-s), 6.90 (1H, dt, J = 2.5 Hz, 6.4 Hz), 7.28-7.30 (3H, m), 7.60 (1H, s), 7.93 (2H, s) I-29 δ 3.92 (2H, s), 6.92 (1H, dt, J = 1.5 Hz, 7.3 Hz), 7.23-7.30 (3H, m), 7.79 (1H, s), 8.04 (2H, s) I-30 δ 3.89 (2H, broad-s), 6.90 (1H, dd, J = 2.4 Hz, 4.9 Hz), 7.23-7.32 (3H, m), 7.61 (1H, s), 7.93 (2H, s) I-31 δ 3.88 (2H, broad-s), 6.90 (1H, d, J = 6.3 Hz), 7.23-7.32 (3H, m), 7.62 (1H, s), 7.92 (2H, s) I-32 δ 6.90-6.94 (1H, m), 7.28-7.33 (3H, m), 7.73 (1H, s), 8.02 (1H, s), 8.25 (1H, s) I-33 δ 2.31 (6H, s), 2.90 (3H, s), 6.81 (1H, dd, J = 1.9 Hz, 7.8 Hz), 7.15- 7.18 (2H, m), 7.30 (1H, t, J = 7.8 Hz), 7.42 (1H, s), 7.52 (2H, s) I-35 δ 0.89 (3H, t, J = 7.3 Hz), 1.23-1.37 (2H, m), 1.54-1.62 (2H, m), 2.70 (2H, t, J = 7.8 Hz), 3.88 (2H, broad), 6.86-6.90 (1H, m), 7.22- 7.30 (3H, m), 7.44 (1H, s), 7.56-7.59 (2H, m). I-36 (DMSO-d₆) δ 0.82 (3H, t, J = 7.3 Hz), 1.19-1.29 (2H, m), 1.44-1.52 (2H, m), 2.66 (2H, t, J = 7.8 Hz), 5.36 (2H, broad-s), 6.75-6.81 (1H, m), 7.12-7.19 (3H, m), 7.58 (1H, s), 7.95 (1H, d, J = 1.5 Hz), 10.02 (1H, s). I-37 (DMSO-d₆) δ 5.37 (2H, s), 6.76-6.80 (1H, m), 7.13-7.19 (3H, m), 8.13 (2H, s), 10.35 (1H, s). I-38 δ 0.79 (3H, t, J = 7.3 Hz), 1.23 (3H, d, J = 6.8 Hz), 1.53-1.63 (2H, m), 2.90-2.99 (1H, m), 3.87 (2H, broad-s), 6.85-6.89 (1H, m), 7.25- 7.29 (3H, m), 7.44 (1H, s), 7.55-7.57 (2H, m). I-39 δ 0.79 (3H, t, J = 7.3 Hz), 1.21 (3H, d, J = 6.8 Hz), 1.50-1.61 (2H, m), 2.91-3.00 (1H, m), 3.88 (2H, broad-s), 6.86-6.91 (1H, m), 7.26- 7.31 (3H, m), 7.51 (2H, s), 7.94 (1H, d, J = 2.0 Hz). I-40 (DMSO-d₆) δ 5.39 (2H, broad-s), 6.77-6.80 (1H, m), 7.13-7.20 (3H, m), 8.02 (2H, s), 10.35 (1H, s). I-41 (DMSO-d₆) δ 5.38 (2H, broad-s), 6.75-6.80 (1H, m), 7.12-7.19 (3H, m), 8.01 (2H, s), 10.34 (1H, s). I-42 (DMSO-d₆) δ 3.34 (3H, s), 5.40 (2H, broad-s), 6.80 (1H, d, J = 7.8 Hz), 7.14-7.21 (3H, m), 8.19 (1H, s), 8.45 (1H, s), 10.36 (1H, s). I-48 (DMSO-d₆) δ 2.48 (3H, s), 5.36 (2H, broad-s), 6.77 (1H, d, J = 7.3 Hz), 7.11-7.18 (3H, m), 7.36 (1H, s), 7.70 (1H, s), 10.09 (1H, s). I-53 δ 0.91 (3H, t, J = 7.3 Hz), 1.57-1.66 (2H, m), 2.69 (2H, t, J = 7.8 Hz), 2.88 (3H, s), 3.97 (1H, s), 6.80 (1H, dd, J = 2.4, 7.8 Hz), 7.19- 7.32 (3H, m), 7.49 (1H, s), 7.60 (1H, s), 7.94 (1H, d, J = 2.0 Hz). I-55 δ 2.73 (3H, s), 3.32 (3H, s), 6.54 (1H, d, J = 8.3 Hz), 6.73 (1H, s), 6.74 (1H, d, J = 8.3 Hz), 6.96 (1H, t, J = 8.3 Hz), 7.77 (2H, s). I-56 δ 2.91 (3H, s), 6.82-6.85 (1H, m), 7.21-7.23 (2H, m), 7.32 (1H, t, J = 7.8 Hz), 7.64 (1H, s), 7.93 (2H, s) I-83 δ 2.38 (6H, s), 2.42 (3H, s), 3.70 (2H, broad), 6.72 (1H, dd, J = 2.4 Hz, 8.1 Hz), 6.89 (1H, d, J = 2.4 Hz), 7.05 (1H, s), 7.07 (1H, d, J = 8.1 Hz), 7.36 (2H, s) I-84 δ 2.37 (6H, s), 3.90 (2H, broad-s), 6.96-7.01 (1H, m), 7.10 (1H, t, J = 7.8 Hz), 7.36 (2H, s), 7.43-7.47 (1H, m), 7.86 (1H, d, J = 13.2 Hz) I-85 δ 2.33 (6H, s), 6.99 (1H, dt, J = 1.5 Hz, 7.8 Hz), 7.10 (1H, t, J = 7.8 Hz), 7.43 (2H, s), 7.46 (1H, d, J = 7.8 Hz), 7.84 (1H, d, J = 13.2 Hz) I-86 δ 2.33 (6H, s), 3.93 (2H, s), 7.05-7.14 (1H, m), 7.17-7.21 (1H, m), 7.31 (1H, s), 7.35 (2H, s), 7.37-7.40 (1H, m) I-87 δ 2.35 (6H, s), 3.74 (2H, broad-s), 6.77-6.83 (1H, m), 7.01 (1H, dd, J = 8.8 Hz, 11.7 Hz), 7.35 (2H, s), 7.42 (1H, dd, J = 2.9 Hz, 6.6 Hz), 8.01 (1H, d, J = 15.6 Hz) I-88 δ 2.40 (6H, s), 4.27 (2H, broad-s), 6.88 (1H, dd, J = 1.5 Hz, 7.8 Hz), 7.03 (1H, dd, J = 1.5 Hz, 7.8 Hz), 7.16 (1H, t, J = 7.8 Hz), 7.29 (1H, s), 7.36 (2H, s) I-89 δ 2.33 (6H, s), 4.27 (2H, broad-s), 7.15 (1H, d, J = 8.1 Hz), 7.35- 7.38 (5H, m) I-90 δ 2.39 (6H, s), 3.85 (2H, broad-s), 6.72 (1H, dd, J = 2.7 Hz, 8.5 Hz), 7.15 (1H, d, J = 2.7 Hz), 7.22 (1H, d, J = 8.5 Hz), 7.36 (2H, s), 7.66 (1H, s) I-91 δ 2.43 (6H, s), 4.34 (2H, broad), 6.86 (1H, dd, J = 1.5 Hz, 8.3 Hz), 6.96 (1H, dd, J = 1.5 Hz, 8.3 Hz), 7.13 (1H, s), 7.19 (1H, t, J = 8.3 Hz), 7.36 (2H, s) I-92 δ 2.44 (6H, s), 3.86 (2H, broad-s), 6.52 (1H, dd, J = 2.9 Hz, 8.5 Hz), 6.91 (1H, d, J = 2.9 Hz), 7.12 (1H, s), 7.35 (2H, s), 7.62 (1H, d, J = 8.5 Hz) I-93 δ 2.27 (6H, s), 4.09 (2H, broad-s), 7.08 (1H, s), 7.33 (2H, s), 7.37 (1H, s), 7.43 (1H, s), 7.83 (1H, s) I-94 (DMSO-d₆) δ 2.29 (3H, s), 2.33 (6H, s), 5.43 (2H, s), 6.57-6.59 (1H, m), 6.85-6.90 (1H, m), 7.01 (1H, t, J = 7.8 Hz), 7.49 (2H, s). I-95 (DMSO-d₆) δ 2.32 (6H, s), 2.76 (3H, d, J = 4.9 Hz), 5.84 (1H, broad), 6.77-6.81 (2H, m), 7.10 (1H, t, J = 7.8 Hz), 7.43 (2H, s), 9.90 (1H, s). I-96 (DMSO-d₆) δ 2.33 (6H, s), 2.76 (3H, d, J = 4.9 Hz), 4.55 (3H, s), 6.58-6.62 (1H, m), 6.70-6.78 (1H, m), 7.13 (1H, t, J = 7.8 Hz), 7.31 (1H, s), 7.50 (2H, s). I-98 (DMSO-d₆) δ 2.32 (6H, s), 2.77 (3H, d, J = 4.9 Hz), 5.82 (1H, broad), 6.79 (1H, t, J = 7.8 Hz), 7.08-7.21 (2H, m), 7.42 (2H, s), 9.88 (1H, s). I-124 (DMSO-d₆) δ 2.26 (6H, s), 7.46 (2H, s), 7.88 (1H, t, J = 7.8 Hz), 8.43-8.48 (2H, m), 8.73 (1H, s), 8.81 (1H, s), 10.27 (1H, s). I-125 δ 2.16 (6H, s), 7.23 (1H, s), 7.53 (2H, s), 7.73 (1H, t, J = 7.8 Hz), 8.45 (1H, d, J = 7.8 Hz), 8.55 (1H, d, J = 7.8 Hz), 9.05 (1H, t, J = 2.0 Hz). I-204 (DMSO-d₆) δ 2.35 (6H, s), 4.31 (2H, broad), 6.84-6.87 (1H, m), 7.21-7.25 (1H, m), 7.29-7.31 (2H, m), 7.47-7.49 (2H, m), 7.83 (1H, s), 8.94 (1H, s). I-351 (DMSO-d₆) δ 2.26 (6H, s), 7.44 (2H, s), 7.51-7.63 (4H, m), 7.74 (1H, d, J = 7.8 Hz), 7.98-8.07 (3H, m), 8.35 (1H, s), 8.71 (1H, s), 9.90 (1H, s), 10.47 (1H, s). I-358 (DMSO-d₆) δ 2.34 (6H, s), 7.21 (1H, dd, J = 8.2, 11.2 Hz), 7.32 (1H, t, J = 7.8 Hz), 7.49-7.56 (4H, m), 7.78 (1H, d, J = 7.8 Hz), 8.04-8.08 (2H, m), 8.23 (1H, s), 8.71 (1H, s), 9.08 (1H, d, J = 11.2 Hz). I-419 (DMSO-d₆) δ 2.34 (6H, s), 7.49-7.63 (6H, m), 7.76 (1H, d, J = 7.8 Hz), 7.99-8.08 (3H, m), 8.37 (1H, s), 9.99 (1H, s), 10.48 (1H, s).

TABLE 12 Comp. No. LC-MS Molecular Ion Peak I-384 573.80 I-385 573.73 I-401 579.67 I-406 516.73 I-414 654.73 I-418 499.87

The insecticide containing the compound represented by Formula (1) of the invention as an active ingredient is suitable for controlling various pests which give damage to paddy rices, fruit trees, vegetables, other crops and flowers and ornamental plants in agricultural, horticultural or stored grain products, or sanitary pests, or for controlling and it may include vermin such as eelworm, for example, those having strong insecticidal effect against Lepidoptera such as cotton caterpillar (Diaphania indica), oriental tea tortrix (Homona magnanima), cabbage webworm (Hellulla undalis), summer fruit tortrix (Adoxophyes orana fasciata), smaller tea tortrix (Adoxophyes sp.), apple tortrix (Archips fuscocupreanus), peach fruit moth (Carposina niponensis), Manchurian fruit moth (Grapholita inopinata), oriental fruit moth (Grapholita molesta), soybean pod borer (Leguminivora glycinivorella), mulberry leafroller (Olethreutes mori), citrus leafminer (Phyllocnistis citrella), persimmon fruit moth (Stathmopoda masinissa), tea leafroller (Caloptilia theivora), (Caloptilia zachrysa), apple leafminer (Phyllonorycter ringoniella), pear barkminer (Spulerrina astaurota), small citrus dog (Papilio xuthus), common cabbage worm (Pieris rapae crucivora), tobacco budworm (Heliothis armigera), codling moth (Cydia pomonella), diamondback moth (Plutella xylostella), apple fruit moth (Argyresthia conjugella), peach fruit moth (Carposina niponensis), rice stem borer (Chilo suppressalis), rice leafroller (Cnaphalocrocis medinalis), tobacco moth (Ephestia elutella), mulberry pyralid (Glyphodes pyloalis), paddy borer (Scirpophaga incertulas), rice skipper (Parnara guttata), rice armyworm (Pseudaletia separata), pink borer (Sesamia inferens), cabbage armyworm (Mamestra brassicae), common cutworm (Spodoptera litura), beet armyworm (Spodoptera exigua), black cutworm (Agrotis ipsilon), turnip moth (Agrotis segetum), beet semi-looper (Autographa nigrisigna), cabbage looper (Trichoplusia ni); Hemiptera such as aster leafhopper (Macrosteles fascifrons), green rice leafhopper (Nephotettix cincticeps), brown rice planthopper (Nilaparvata lugens), small brown planthopper (Laodelphax striatellus), whitebacked rice planthopper (Sogatella furcifera), citrus psylla (Diaphorina citri), grape whitefly (Aleurolobus taonabae), silverleaf whitefly (Bermisia argentifolii), sweetpotato whitefly (Bemisia tabaci), greenhouse whitefly (Trialeurodes vaporariorum), turnip aphid (Lipaphis erysimi), cotton aphid (Aphis gossypii), apple aphid (Aphis Citricola), green peach aphid (Myzus persicae), Indian wax scale (Ceroplastes ceriferus), Comstock mealybug (Pseudococcus Comstocki), Japanease mealybug (Planococcus kraunhiae), cottony citrus scale (Pulvinaria aurantii), camphor scale (Pseudaonidia duplex), san Jose scale (Comstockaspis perniciosa), arrowhead scale (Unaspis yanonensis), brownwinged green bug (Plautia Stali), brown marmorated stink bug (Halyomorpha mista); Coleoptera such as soybean beetle (Anomala rufocuprea), Japanese beetle (Popillia japonica), cigarette beetle (Lasioderma serricorne), powderpost beetle (Lyctusbrunneus), twenty-eight-spotted ladybird (Epilachna vigintioctopunctata), adzuki bean weevil (Callosobruchus chinensis), vegetable weevil (Listroderes costirostris), maize weevil (Sitophilus zeamais), boll weevil (Anthonomus grandis), rice water weevil (Lissorhoptrus oryzophilus), cucurbit leaf beetle (Aulacophora femoralis), rice leaf beetle (Oulema oryzae), striped flea beetle (Phyllotreta striolata), pine shoot beetle (Tomicus piniperda), Colorado potato beetle (Leptinotarsa decemlineata), Mexican bean beetle (Epilachna varivestis), corn rootworm (Diabrotica sp.), yellowspotted longicorn beetle (Psacothea hilaris), whitespotted longicorn beetle (Anoplophora malasiaca); Diptera such as melon fly (Dacus(Bactrocera) dorsalis), rice leafminer (Agromyza oryzae), onion maggot (Delia antiqua), seedcorn maggot (Delia platura), soybean pod gall midge (Asphondylia sp.), house fly (Musca domestica), garden pea leafminer (Chromatomyia horticola), legume leafminer (Liriomyza trifolii), bryony leafminer (Liriomyza bryoniae), common house mosquito (Culex pipiens); Nematoda such as coffee root-lesion nematode (Pratylenchus coffeae), root-lesion nematode (Pratylenchus sp.), potato cyst nematode (Globodera rostochiensis), root-knot nematode (Meloidogyne sp.), citrus nematode (Tylemchulus semipenetrans), nematode (Aphelenchus avenae), chrysanthemum foliar nematode (Aphelenchoides ritzemabosi); Thysanoptera such as melon thrips (Thrips palmi), western flower thrips (Frankliniella occidentalis), yellow tea thrips (Scirtothrips dorsalis), honeysuckle thrips (Thrips flavus), onion thrips (Thrips tabaci); Orthoptera such as German cockroach (Blattella germanica), American cockroach (Periplaneta americana), rice grasshopper (Oxya yezoensis) and the like.

The insecticides containing the compound represented by Formula (1) of the invention as an active ingredient have notable insecticidal effect against the above-described pests that damage various lowland crops, upland crops, fruit trees, vegetables, other crops and horticultural products. Thus, the insecticidal effect of the invention can be obtained by treating the paddy field water, plant stems and leaves, or soil of the crops of lowland, upland, fruit trees, vegetables, other crops, and flowers and ornamental plants, during the seasons expected of the appearance of such pests, or before or at the point of pest appearance.

The insecticides of the invention are in general used in appropriate formulation forms according to the use, prepared by conventional methods for preparation of agricultural and horticultural chemicals. That is, the compounds represented by Formula (1) may be used in suitable formulations, such as a suspension, an emulsion, a liquid formulation, a water-dispersible powder, a granule, a dust formulation, tablets and the like, prepared by blending the compounds with suitable inert carriers, or with auxiliary agents if necessary, in appropriate proportions, followed by dissolution, separation, suspension, mixing, impregnation, adsorption or adhesion of the ingredients.

The inert carrier that can be used in the invention may be solids or liquids and include, in particular, soybean powders, grain powders, wood powders, bark powders, coarse powders, tobacco powders, walnut shell powders, brans, cellulose powders, residues from plant extraction, synthetic polymers such as pulverized synthetic resins, clays (for example, kaolin, bentonite, acidic white clay), talc (for examples, talc, pyrophyllite, etc.), silica (for examples, diatomite, sand, mica, white carbon (hydrous silica powders, hydrous silica powders called synthetic high dispersity silicic acids, there are also products containing calcium silicate as main component)), activated carbon, sulfur powder, pumice, calcined diatomaceous powders, pulverized bricks, fly ash, sand, inorganic mineral powders such as calcium carbonate and calcium phosphate, chemical fertilizers such as ammonium sulfate, ammonium phosphate, ammonium nitrate, urea and ammonium chloride, a compost and the like, which are used alone or as mixtures of two or more.

Materials that can be used as the inert carrier for liquids are selected from those having the function as solvent, as well as those capable of dispersing the active ingredient compound under an aid of an auxiliary agent even if the inert carrier has not the function as solvent, and they can be exemplified by, for example, the carriers listed below: water, alcohols (e.g., methanol, ethanol, isopropanol, butanol, ethylene glycol, etc.), ketones (e.g., acetone, methyl ethyl ketone, methyl isobutyl ketone, diisobutylketone, cyclohexanone, etc.), ethers (e.g., diethyl ether, dioxane, cellosolve, diisopropyl ether, tetrahydrofuran, etc.), aliphatic hydrocarbons (e.g., kerosene, mineral oil, etc.), aromatic hydrocarbons (e.g., benzene, toluene, xylene, solvent naphtha, alkyl naphthalene, etc.), halogenated hydrocarbons (e.g., dichloromethane, chloroform, tetrachlorocarbon, chlorobenzene, etc.), esters (e.g., ethyl acetate, butyl acetate, ethyl propionate, diisobutyl phthalate, dibutyl phthalate, dioctyl phthalate, etc.), amides (e.g., dimethyl formamide, diethyl formamide, dimethyl acetamide, etc.), and nitriles (e.g., acetonitrile, etc.), which are used alone or as mixtures of two or more.

The auxiliary agent may include the following representative auxiliary agents, which are used alone or in combination of two or more of them depending on the purpose; however, it is also possible not to use any auxiliary agent.

For the purpose of emulsification, dispersion, solubilization and/or wetting of the active ingredient compound, surfactants can be used, for example, polyoxyethylene alkyl ethers, polyoxyethylene alkyl aryl ethers, polyoxyethylene higher fatty acid esters, polyoxyethylene resin acid esters, polyoxyethylene sorbitan monolaurate, polyoxyethylene sorbitan monooleates, alkyl aryl sulfonate, naphthalene sulfonate, lignin sulfonate, higher alcohol sulfonate esters and the like.

For the purpose of dispersion stabilization, adhesion and/or binding of the active ingredient compound, the following auxiliary agent can be use, for example, casein, gelatin, starch, methyl cellulose, carboxymethyl cellulose, gum Arabic, polyvinyl alcohol, pine root oil, corn oil, bentonite, xanthan gum, lignin sulfonate salts and the like.

For the purpose of improving the flowability of solid products, the auxiliary agents can be used, for example, wax, stearic acid salts, phosphoric alkyl esters and the like. An auxiliary agent such as a naphthalene sulfonate condensation product, or a condensed phosphate salt can be used as a suspending agent in suspensions. An antifoaming agent such as silicone oils can be also used as an auxiliary agent.

In addition, the compound represented by Formula (1) of the invention is stable against light, heat, oxidation and the like, but if desired, more stable compositions may obtained by adding a stabilizer. The stabilizer may include, for example, antioxidants or UV absorbents, phenol derivatives such as BHT (2,6-di-t-butyl-4-methyl phenol), BHA (butyl hydroxy anisole), bisphenol derivatives, and aryl amines such as phenyl-α-naphthyl amine, phenyl-β-naphthyl amine, condensation product of phenetidine and acetone, or benzophenone compounds.

The effective amount of the compound represented by Formula (1) of the invention is typically 0.5 to 20% by weight in a dust formulation, 5 to 50% by weight in an emulsion, 10 to 90% by weight in a water-dispersible powder, 0.1 to 20% by weight in a granule, and 10 to 90% by weight in a flowable formulation. Meanwhile, the amount of carrier in the respective formulations is typically 60 to 99% by weight in a dust formulation, 40 to 95% by weight in an emulsion, 10 to 90% by weight in a water-dispersible powder, 80 to 99% by weight in a granule, and 10 to 90% by weight in a flowable formulation. The amount of such auxiliary agent is typically 0.1 to 20% by weight in a dust formulation, 1 to 20% by weight in an emulsion, 0.1 to 20% by weight in a water-dispersible powder, 0.1 to 20% by weight in a granule, and 0.1 to 20% by weight in a flowable formulation.

In order to control various pests, an amount effective for blight control can be applied, just as it is, or as an adequate dilution with water, or as a suspension, to the crops expected of the appearance of the corresponding pests or to the places where such occurrence is not preferable. The amount of use depends on various factors such as, for example, the purpose, the pest to be controlled, the state of plant growth, trend of pest appearance, climate, environmental conditions, formulation, method of use, place of use, timing of use and the like, but it is preferable to use the active ingredient in the concentration of 0.0001 to 5000 ppm, and preferably 0.01 to 1000 ppm. The dose that can be used in approximately 10 a is generally in the range of 1 to 300 g of the active ingredient.

The insecticide of the invention containing the compound represented by Formula (1) as an active ingredient may be used alone in control of various pests in agricultural, horticultural and stored grain products, which damage the rice plants, fruit trees, vegetables, other crops and flowers, or sanitary pests or eelworms, and further in order to obtain superior control effect with respect to various pests which occur at the same time, it may be used in combination with at least one other insecticide and/or fungicide.

Examples of other insecticides which can be combined with the compound represented by Formula (1) of the invention may include, for example, pyrethroid insecticides such as allethrin, tetramethrin, resmethrin, phenothrin, furamethrin, permethrin, cypermethrin, deltamethrin, cyhalothrin, cyfluthrin, fenpropathrin, tralomethrin, cycloprothrin, flucythrinate, fluvalinate, acrinathrin, tefluthrin, bifenthrin, empenthrin, beta-cyfluthrin, zeta-cypermethrin, fenvalerate and the like, and various isomers thereof; or Dalmatian pyrethrum extract; organophosphate insecticides such as DDVP, cyanophos, fenthion, fenitrothion, tetrachlorvinphos, dimethylvinphos, propaphos, methylparathion, temephos, phoxim, acephate, isofenphos, salithion, DEP, EPN, ethion, mecarbam, pyridafenthion, diazinon, pirimiphos-methyl, etrimfos, isoxathion, quinalphos, chlorpyrifos-methyl, chlorpyrifos, phosalone, phosmet, methidathion, oxydeprofos, vamidothion, malathion, phenthoate, dimethoate, formothion, thiometon, disulfoton, phorate, terbufos, profenofos, prothiofos, sulprofos, pyraclofos, monocrotofos, naled, fosthiazate, cadusafos; carbamate insecticides such as NAC, MTMC, MIPC, BPMC, XMC, PHC, MPMC, ethiofencarb, bendiocarb, pirimicarb, carbosulfan, benfuracarb, methomyl, oxamyl, aldicarb; arylpropylether insecticides such as etofenprox, halfenprox; silylether compounds such as silafluofen; insecticidal natural products such as nicotine-sulfate, polynactins, abamectin, milbemectin, BT; insecticides such as cartap, thiocyclam, bensultap, diflubenzuron, chlorfluazuron, teflubenzuron, triflumuron, flufenoxuron, flucycloxuron, hexaflumuron, fluazuron, imidacloprid, nitenpyram, acetamiprid, dinotefuran, pymetrozine, fipronil, buprofezin, fenoxycarb, pyriproxyfen, methoprene, hydroprene, kinoprene, endosulfan, diafenthiuron, triazamate, tebufenozide, benzoepin; acaricides such as dicofol, chlorobenzilate, phenisobromolate, tetradifon, CPCBS, BPPS, chinomethionate, amitraz, benzomate, hexythiazox, fenbutatin oxide, cyhexatin, dienochlor, clofentezine, pyridaben, fenpyroximate, fenazaquin, tebufenpyrad; novaluron, noviflumuron, emamectin benzoate, clothianidin, thiacloprid, thiamethoxam, flupyrazofos, acequinocyl, bifenazate, chromafenozide, etoxazole, fluacrypyrim, flufenzine, halofenozide, indoxacarb, methoxyfenozide, spirodiclofen, tolfenpyrad, gamma-cyhalothrin, ethiprole, amidoflumet, bistrifluoron, flonicamid, flubrocythrinate, flufenerim, pyridalyl, pyrimidifen, spinosad, or spiromesifen.

Examples of the fungicides which can be combined with the compound represented by Formula (1) of the invention may include, for example, azole fungicides such as triadimefon, hexaconazole, propiconazole, ipconazole, prochloraz, triflumizole; pyrimidine fungicides such as pyrifenox, fenarimol; anilinopyrimidine fungicides such as mepanipyrim, cyprodinil; acylalanine fungicides such as metalaxyl, oxadixyl, benalaxyl; benzimidazole fungicides such as thiophanate-methyl, benomyl; dithiocarbamate fungicides such as mancozeb, propineb, zineb, metiram; organochlorine fungicides such as tetrachloroisophthalonitrile; carboxamide fungicides such as carpropamid, ethaboxam; morpholine fungicides such as dimethomorph; strobilurin fungicides such as azoxystrobin, kresoxim-methyl, metominostrobin, orysastrobin, fluoxastrobin, trifloxystrobin, dimoxystrobin, pyraclostrobin, picoxystrobin; dicarboximide fungicides such as iprodione, procymidone; soil-applied fungicides such as flusulfamide, dazomet, methyl isothiocyanate, chloropicrin; copper fungicides such as basic copper chloride, basic copper sulfate, copper nonylphenol sulfonate, oxine-copper; inorganic fungicides such as sulfur, zinc sulfate; organophosphate fungicides such as edifenphos, tolclofos-methyl, fosetyl; melanin biosynthesis inhibitors such as phthalide, tricyclazole, pyroquilon, diclocymet; antibiotics such as kasugamycin, validamycin, polyoxins; fungicidal natural products such as rape seed oil; fungicides such as benthiavalicarb-isopropyl, iprovalicarb, cyflufenamid, fenhexamid, quinoxyfen, spiroxamine, diflumetorim, metrafenone, picobenzamid, proquinazid, silthiofam, oxpoconazole, famoxadone, cyazofamid, fenamidone, furametpyr, zoxamide, boscalid, tiadinil, simeconazole, chlorothalonil, cymoxanil, captan, dithianon, fluazinam, folpet, dichlofluanid, (RS)—N-[2-(1,3-dimethylbutyl)thiophen-3-yl]-1-methyl-3-trifluoro methyl-1H-pyrazole-4-carboxamide (penthiopyrad: ISO proposed), oxycarboxin, mepronil, flutolanil, triforine, oxolinic acid, probenazole, acibenzolar-S-methyl, isoprothiolane, ferimzone, diclomezine, pencycuron, fluoroimide, chinomethionate, iminoctadine-triacetate, iminoctadine-albesilate and the like.

When the compound represented by Formula (1) of the invention is used in combination with at least one other insecticide and/or fungicide, a mixed composition of the compound represented by Formula (1) and other insecticide and/or fungicide may be used, or the compound represented by Formula (1) and other insecticide/fungicide may be mixed and used at the time of apply.

In addition to the above-mentioned insecticides and fungicides, the compound represented by Formula (1) can be mixed with plant protecting agents such as a herbicide, a fertilizer, a soil reformer, a plant growth controlling agent and a material, in order to form multi-purpose compositions of high efficacy, which are expected to provide an additive effect or a synergistic effect.

The following Examples illustrate representative Examples of the invention, but they are not intended to limit the invention.

Example 1-1 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-nitrobenzamide

To a solution prepared by adding 20.0 g of 2,6-dimethyl-4-heptafluoroisopropylaniline and 11.0 g of pyridine to 100 ml of tetrahydrofuran at room temperature with stirring, 13.0 g of 3-nitrobenzoyl chloride dissolved in 20 ml of tetrahydrofuran was gradually added dropwise thereto. After the reaction solution was stirred at room temperature for 10 hours, ethyl acetate and water were added thereto. Phase separation was carried out, and then the organic layer was separated and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled off under reduced pressure. Thus obtained residue was washed with a solvent mixture of hexane-diisopropyl ether to give 26.0 g (yield 85%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.33 (6H, s), 7.37 (2H, s), 7.68 (1H, s), 7.72 (1H, t, J=8.1 Hz), 8.28 (1H, d, J=8.1 Hz), 8.44 (1H, dd, J=1.2, 8.1 Hz), 8.75 (1H, t, J=1.2 Hz).

Example 1-2 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzamide (Compound No. I-2)

To a solution prepared by adding 0.90 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-nitrobenzamide and 1.56 g of anhydrous tin(II) chloride to 25 ml of ethanol at room temperature with stirring, 2 ml of concentrated hydrochloric acid was added and the mixture was stirred at 60° C. for one hour. After brought back to room temperature, the reaction solution was poured onto water, and neutralization was carried out using potassium carbonate. Ethyl acetate was added, the insolubles were filtered off, and then the organic layer was separated and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled off under reduced pressure. Thus obtained residue was washed with hexane to give 0.44 g (yield 53%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.34 (6H, s), 3.87 (2H, broad), 6.86-6.89 (1H, m), 7.20-7.35 (6H, m)

Example 1-3 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(benzoylamino)benzamide (Compound No. 10)

To a solution prepared by adding 0.25 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzamide and 0.06 g of pyridine to 5 ml of tetrahydrofuran at room temperature with stirring, 0.09 g of benzoyl chloride dissolved in 1 ml of tetrahydrofuran was added dropwise. After stirring at room temperature for 1 hour, ethyl acetate and 1N hydrochloric acid were added to the reaction solution, and the organic layer was separated. The organic layer was washed once with saturated aqueous sodium hydrogen carbonate solution and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled off under reduced pressure. Thus obtained solid was washed with diisopropyl ether to give 0.29 g (yield 92%) of the title compound as a white solid.

¹H-NMR (DMSO-d₆, ppm) δ 2.37 (6H, s), 7.34 (2H, s), 7.46-7.57 (4H, m), 7.75 (1H, d, J=7.8 Hz), 7.98-8.01 (2H, m), 8.12 (1H, d, J=7.3 Hz), 8.34 (1H, s), 8.87 (1H, s), 9.66 (1H, s).

Example 2-1 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl-N-methyl 3-nitrobenzamide

To a suspension of 0.18 g of 60% sodium hydride in 15 ml of tetrahydrofuran, 2.0 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-nitrobenzamide dissolved in 5 ml of tetrahydrofuran was added dropwise at room temperature. After the mixture was stirred at room temperature for 30 minutes, 0.65 g of methyl iodide dissolved in 5 ml of tetrahydrofuran was added dropwise. Then, after raising temperature to 50° C. and stirred for 4 hours, the reaction solution was returned to room temperature, and ethyl acetate and water were added. The organic layer was separated, washed once with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=6:1) to give 1.73 g (yield 84%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.31 (6H, s), 3.38 (3H, s), 7.27 (2H, s), 7.37 (1H, t, J=7.8 Hz), 7.62-7.65 (1H, m), 8.05 (1H, t, J=2.0 Hz), 8.11-8.14 (1H, m).

Example 2-2 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl-N-methyl 3-aminobenzamide (Compound No. I-5)

A solution prepared by adding 1.50 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl-N-methyl 3-nitrobenzamide and 0.15 g of 10% palladium-carbon to 20 ml of methanol, was stirred under a hydrogen atmosphere at atmospheric pressure for 2 hours. After the catalyst was filtered off, the solvent was distilled off under reduced pressure. Then, thus obtained solid was washed with hexane to give 1.24 g of the title compound (yield 88%) as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.27 (6H, s), 3.31 (3H, s), 3.80 (2H, broad), 6.40-6.43 (1H, m), 6.54-6.58 (1H, m), 6.71 (1H, t, J=2.0 Hz), 6.76-6.86 (1H, m), 7.22 (2H, s).

Example 2-3 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl-N-methyl 3-(benzoylamino)benzamide (Compound No. 1478)

The title compound, was prepared as a white solid according to the conditions described in Example 1-3.

¹H-NMR (DMSO-d₆, ppm) δ 2.29 (6H, s), 3.24 (3H, s), 6.84 (1H, d, J=7.8 Hz), 7.12 (1H, t, J=7.8 Hz), 7.33 (2H, s), 7.50-7.64 (4H, m), 7.85-7.88 (2H, m), 7.98-8.03 (1H, m), 10.22 (1H, s).

Example 3 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-[(2-chloropyridin-3-yl)carbonylamino]benzamide (Compound No. 106)

To a solution prepared by adding 0.6 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzamide and 0.4 g of pyridine to 10 ml of tetrahydrofuran, 0.35 g of 2-chloronicotinoyl chloride hydrochloride was added and the mixture was stirred at room temperature for 4 hours. Ethyl acetate was added, the mixture was twice washed with saturated sodium hydrogen carbonate solution, and the solvent was distilled off under reduced pressure. Thus obtained solid was washed with a solvent mixture of hexane-diisopropyl ether and dried to give 0.64 g (yield 75%) of the title compound as a white solid.

¹H-NMR (DMSO-d₆, ppm) δ 2.30 (6H, s), 7.45 (2H, s), 7.54-7.60 (2H, m), 7.77-7.80 (1H, m), 7.95 (1H, d J=7.8 Hz), 8.10-8.12 (1H, m), 8.30 (1H, s), 8.54-8.59 (1H, m), 10.03 (1H, s), 10.88 (1H, s).

Example 4 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-[(pyridin-3-yl)carbonylamino]benzamide (Compound No. 101)

A solution prepared by adding 99 mg of nicotinic acid and 153 mg of 1,1′-oxalyl diimidazole to 10 ml of acetonitrile was stirred at room temperature for 15 minutes and again at 40° C. for 40 minutes. After returning back to room temperature, 300 mg of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzamide was added, and the mixture was stirred at 60° C. for 5 hours. Then, the solvent was distilled off under reduced pressure, and to the residue obtained therefrom, ethyl acetate was added. The organic layer was twice washed with saturated sodium hydrogen carbonate solution, and the solvent was again distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent: hexane:ethyl acetate=1:3) to give 70 mg (yield 18%) of the title compound as a white solid.

¹H-NMR (DMSO-d₆, ppm) δ 2.30 (6H; s), 7.45 (2H, s), 7.54-7.61 (2H, m), 7.78 (1H, d, J=8.3 Hz), 8.06 (1H, d, J=7.3 Hz), 8.32-8.35 (2H, m), 8.77-8.79 (1H, m), 9.15 (1H, d, J=1.5 Hz), 10.00 (1H, s), 10.66 (1H, s).

Example 5-1 Preparation of N-methyl-2-bromo-4-heptafluoroisopropyl-6-methylaniline

To a solution prepared by adding 1.0 g of N-methyl-4-heptafluoroisopropyl-2-methylaniline to 5 ml of N,N-dimethyl formamide, 0.8 g of N-bromosuccinimide dissolved in 3 ml of N,N-dimethyl formamide was added dropwise. After the mixture was stirred at room temperature for 5 hours, ethyl acetate and water were added, and the organic layer was separated. The organic layer was twice washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent: hexane:ethyl acetate=9:1) to give 0.86 g (yield 68%) of the title compound as a red oil.

¹H-NMR (CDCl₃, ppm) δ 2.41 (3H, s), 2.93 (3H, s), 3.90 (1H, broad), 7.23 (1H, s), 7.54 (1H, s).

Example 5-2 Preparation of N-(2-bromo-4-heptafluoroisopropyl-6-methyl)phenyl-N-methyl 3-(benzoylamino)benzamide (Compound No. 1479)

The title compound was prepared as a white solid from N-methyl-2-bromo-4-heptafluoroisopropyl-6-methylaniline according to the conditions described in Examples 1-2 and 1-3.

¹H-NMR (DMSO-d₆, ppm) δ 2.41 (3H, s), 3.25 (3H, s), 6.95 (1H, dd, J=1.5, 7.8 Hz), 7.16 (1H, t, J=7.8 Hz), 7.50-7.64 (4H, m), 7.68 (1H, s), 7.86-7.88 (2H, m), 7.93 (1H, t, J=1.5 Hz), 7.98-8.00 (1H, m), 10.24 (1H, s).

Example 6 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl-N-methyl 3-(N-methylbenzoylamino)benzamide (Compound No. 1487)

To a suspension of 40 mg of 60% sodium hydride in 10 ml of tetrahydrofuran, 0.3 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl-N-methyl 3-(benzoylamino)benzamide dissolved in 5 ml of tetrahydrofuran was added dropwise at room temperature. After the mixture was stirred at room temperature for 1 hour, 0.16 g of methyl iodide dissolved in 5 ml of tetrahydrofuran was added dropwise. Then, after returning to a temperature to 50° C. and stirred for 4 hours, the reaction solution was returned to room temperature, and ethyl acetate and water were added to the reaction solution. The organic layer was separated, washed once with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Thus obtained residue was washed with diisopropyl ether to give 1.73 g (yield 84%) of the title compound as a white solid.

¹H-NMR (DMSO-d₆, ppm) δ 2.20 (6H, s), 3.08 (3H, s), 3.20 (3H, s), 6.93-7.39 (10H, m), 7.45-7.51 (1H, m).

Example 7-1 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzthioamide

0.35 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzamide and 0.19 g of Lawesson's reagent was added to 10 ml of toluene, and the mixture was heated with stirring at reflux temperature for 6 hours. The reaction solution was concentrated under reduced pressure, the solvent was distilled off, and thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=3:1) to give 0.07 g (yield 20%) of the title compound.

¹H-NMR (CDCl₃, ppm) δ 2.36 (6H, s), 3.87 (2H, broad-s), 6.84-6.87 (1H, m), 7.18-7.24 (2H, m), 7.33 (1H, s), 7.39 (2H, s), 8.56 (1H, broad-s).

Example 7-2 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(benzoylamino)benzthioamide (Compound No. 2201)

The title compound was prepared from N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzthioamide according to the conditions described in Example 1-3.

¹H-NMR (CDCl₃, ppm) δ 2.38 (6H, s), 7.25-8.00 (11H, m), 8.34 (1H, s), 8.85 (1H, broad.).

Example 8 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(phenylthiocarbonylamino)benzamide (Compound No. 2202) and N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(phenylthiocarbonylamino)benzthioamide (Compound No. 2203)

A solution of 0.37 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(benzoylamino)benzamide and 0.30 g of Lawesson's reagent in 10 ml of toluene was stirred at 70° C. for 6 hours. The reaction solution was concentrated under reduced pressure, and thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=3:1) to give 0.18 g (yield 47%) of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(phenylthiocarbonylamino)benzamide and 0.05 g (yield 13%) of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(phenylthiocarbonylamino)benzthioamide.

Characterization of Compound No. 2202

¹H-NMR (CDCl₃, ppm) δ 2.36 (6H, s), 7.37 (2H, s), 7.47-7.61 (5H, m), 7.85-8.03 (4H, m), 8.57 (1H, s), 9.18 (1H, s).

Characterization of Compound No. 2203

¹H-NMR (CDCl₃, ppm) δ 2.38 (6H, s), 7.41 (2H, s), 7.45-7.55 (4H, m), 7.90-7.96 (4H, m), 8.57 (1H, broad), 8.74 (1H, broad), 9.18 (1H, broad).

Example 9-1 Preparation of N-benzyl-N-(2,6-dimethyl-4-heptrafluoroisopropyl)phenyl 3-nitrobenzamide

The title compound was prepared from N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-nitrobenzamide and benzyl bromide according to the process described in Example 6.

Example 9-2 Preparation of N-benzyl-N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(2-fluorobenzoylamino)benzamide

The title compound was prepared from N-benzyl-N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-nitrobenzamide and 2-fluorobenzoyl chloride according to the processes described in Examples 1-2 and 1-3.

Example 9-3 Preparation of N-benzyl-N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-[N-ethyl-N-(2-fluorobenzoyl)amino]benzamide

The title compound was prepared from N-benzyl-N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(2-fluorobenzoylamino)benzamide and ethyl iodide according to the process described in Example 6.

Example 9-4 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-[N-ethyl-N-(2-fluorobenzoyl)amino]benzamide (Compound No. 1206)

A solution of 1.07 g of N-benzyl-N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-[N-ethyl-N-(2-fluorobenzoyl)amino]benzamide and 0.15 g of 10% palladium-carbon in 10 ml of methanol was stirred at 45° C. for 6 hours under a hydrogen atmosphere. The catalyst was filtered off, and the solvent was distilled off under reduced pressure. Then, thus obtained residue was purified by silica gel (Fuji Silysia Chemical Ltd., NH silica) column chromatography (eluent:hexane:ethyl acetate=1:1) to give 0.30 g (yield 32%) of the title compound as a white solid.

¹H-NMR (DMSO-d₆, ppm) δ 1.17 (3H, broad), 2.22 (6H, s), 3.99 (2H, broad), 7.01-7.08 (2H, m), 7.29-7.43 (6H, m), 7.72-7.77 (2H, m), 9.90 (1H, s).

Example 10-1 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 2-fluoro-3-nitrobenzamide

2.35 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 2-chloro-3-nitrobenzamide prepared according to the process described in Example 1-1 and 0.87 g of potassium fluoride (spray-dried product) were added to 25 ml of N,N-dimethyl formamide dried by molecular sieves, and the mixture was heated with stirring at 150° C. for 3 hours. After the reaction solution was brought back to room temperature, ethyl acetate and water were added thereto, and phase separation was carried out. The organic layer was separated, washed twice with water and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel chromatography (eluent:hexane:ethyl acetate=4:1) to give 1.02 g (yield 45%) of the title compound as a solid.

¹H-NMR (CDCl₃, ppm) δ 2.37 (6H, s), 7.39 (2H, s), 7.48-7.53 (1H, m), 7.87 (1H, d, J=11.5 Hz), 8.23-8.28 (1H, m), 8.42-8.46 (1H, m).

Example 10-2 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(benzoylamino)-2-fluorobenzamide (Compound No. 601)

The title compound was prepared according to the processes described in Examples 1-2 and 1-3.

¹H-NMR (DMSO-d₆, ppm) δ 2.34 (6H, s), 7.37 (1H, t, J=7.8 Hz), 7.45 (2H, s), 7.53-7.65 (4H, m), 7.77-7.82 (1H, m), 8.00-8.02 (2H, m), 10.10 (1H, s), 10.29 (1H, s).

Example 11-1 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 4-fluoro-3-nitrobenzamide

5.22 g of 4-fluoro-3-nitrobenzoic acid and 0.1 g of N,N-dimethyl formamide were introduced to 30 ml of toluene, and 3.7 g of thionyl chloride was added. The reaction mixture was stirred at 80° C. for 1 hour and again for 2 hours under reflux conditions. After cooling to room temperature, the solvent was distilled off under reduced pressure, thus obtained residue was dissolved in 10 ml of tetrahydrofuran, and this solution was added dropwise to a mixed solution of 8.1 g of 2,6-dimethyl-4-heptafluoroisopropylaniline, 4.4 g of pyridine and 20 ml of tetrahydrofuran. After the mixture was stirred for 2 hours, ethyl acetate was introduced, and the organic layer was washed with water and saturated sodium hydrogen carbonate solution sequentially. The organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=4:1) to give 5.9 g (yield 46%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.11 (6H, s), 7.26-7.31 (3H, m), 8.12-8.15 (1H, m), 8.60-8.62 (1H, m), 8.70 (1H, s).

Example 11-2 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-amino-4-fluorobenzamide

The title compound was prepared according to the conditions described in Example 1-2. The compound was obtained as a white solid.

¹H-NMR (DMSO-d₆, ppm) δ 2.26 (6H, s), 5.42 (2H, broad-s), 7.10-7.19 (2H, m), 7.37 (1H, dd, J=2.0, 8.8 Hz), 7.42 (2H, s), 9.78 (1H, s).

Example 11-3 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 4-fluoro-3-(methylamino)benzamide

18 ml of 98% sulfuric acid was cooled to a temperature of 0° C. to 5° C. and stirred, and 2.50 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-amino-4-fluorobenzamide was added thereto. After the reaction mixture was stirred for 15 minutes, 18 ml of an aqueous solution of 37% formaldehyde was added dropwise, and the mixture was stirred at 0° C. for 1 hour and for further 3 hours at room temperature. To the reaction solution cooled again to 0° C., 28% ammonia solution in water was added to neutralize the solution, ethyl acetate was added, and the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=4:1) to give 1.74 g (yield 67%) of the title compound in an amorphous form.

¹H-NMR (CDCl₃, ppm) δ 2.32 (6H, s), 2.94 (3H, d, J=4.9 Hz), 4.14 (1H, broad), 7.03 (1H, dd, J=8.3, 11.2 Hz), 7.10-7.13 (1H, m), 7.24 (1H, s), 7.34 (2H, s), 7.42 (1H, s).

The following compounds were prepared according to the process described in Example 11-3:

N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 2-fluoro-3-(methylamino)benzamide

¹H-NMR (DMSO-d₆) δ 2.32 (6H, s), 2.76 (3H, d, J=4.9 Hz), 5.84 (1H, broad), 6.77-6.81 (2H, m), 7.10 (1H, t, J=7.8 Hz), 7.43 (2H, s), 9.90 (1H, s).

N-[2,6-dimethyl-4-(nonafluoro-2-butyl)]phenyl 2-fluoro-3-(methylamino)benzamide

¹H-NMR (DMSO-d₆) δ 2.32 (6H, s), 2.77 (3H, d, J=4.9 Hz), 5.82 (1H, broad), 6.79 (1H, t, J=7.8 Hz), 7.08-7.21 (2H, m), 7.42 (2H, s), 9.88 (1H, s).

N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl-N-methyl 2-fluoro-3-(methylamino)benzamide

¹H-NMR (DMSO-d₆) δ 2.33 (6H, s), 2.76 (3H, d, J=4.9 Hz), 4.55 (3H, s), 6.58-6.62 (1H, m), 6.70-6.78 (1H, m), 7.13 (1H, t, J=7.8 Hz), 7.31 (1H, s), 7.50 (2H, s).

Example 11-4 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 4-fluoro-3-[N-methyl-N-(4-nitrobenzoyl)amino]benzamide (Compound No. 1464)

The title compound was obtained as a white solid using 4-nitrobenzoyl chloride according to the conditions described in Example 1-3.

¹H-NMR (DMSO-d₆, ppm) δ 2.23 (6H, s), 3.42 (3H, s), 7.41 (¹H, broad), 7.45 (2H, s), 7.60 (2H, broad), 7.90 (1H, broad), 8.08-8.13 (3H, broad), 9.93 (1H, s).

Example 12-1 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 6-chloropyridine-2-carboxamide

A mixture of 2.2 g of 6-chloropyridine-2-carboxylic acid and 0.1 g of N,N-dimethyl formamide was introduced to 10 ml of toluene, and then 2.0 g of thionyl chloride was added thereto. After stirred at 80° C. for 1 hour, the reaction mixture was stirred for another 2 hours under reflux conditions. The mixture was cooled to room temperature, the solvent was distilled off under reduced pressure, and thus obtained residue was added dropwise to a mixed solution of 3.67 g of 2,6-dimethyl-4-heptafluoroisopropylaniline, 1.22 g of pyridine and 20 ml of tetrahydrofuran. After the mixture was stirred at room temperature for 2 hours, ethyl acetate was added thereto, and the organic layer was washed with water and saturated aqueous sodium hydrogen carbonate solution sequentially. The organic layer was dried over anhydrous magnesium sulfate, the solvent was distilled off under reduced pressure, and thus obtained residue was washed with cooled hexane at 5° C. to give 4.42 g (yield 77%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.36 (6H, s), 7.36 (2H, s), 7.56 (1H, dd, J=1.0, 8.1 Hz), 7.88 (1H, dd, J=7.6, 8.1 Hz), 8.23 (1H, dd, J=1.0, 7.6 Hz), 9.27 (1H, broad-s).

Example 12-2 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 6-aminopyridin-2-carboxamide

A mixture of 3.08 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 6-chloropyridin-2-carboxamide, 30 ml of 28% ammonia solution in water, 0.20 g of copper sulfate and 70 ml of methanol was introduced into a 200 ml autoclave and was heated with stirring at 150° C. for 2 hours. After the mixture was cooled to room temperature, ammonia was distilled off at 60° C. and atmospheric pressure, and methanol was distilled off under reduced pressure. Ethyl acetate and water were added to the reaction solution, phase separation was carried out, and the organic layer was separated and dried over anhydrous sodium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=3:2 to 2:3) to give 2.90 g (yield 98%) of the title compound as an oil.

¹H-NMR (CDCl₃, ppm) δ 2.35 (6H, s), 4.57 (2H, broad-s), 6.69-6.74 (1H, m), 7.34 (2H, s), 7.62-7.66 (2H, m), 9.39 (1H, broad-s).

Example 12-3 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 6-(benzoylamino)pyridin-2-carboxamide (Compound No. 2001)

A mixture of 0.16 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 6-aminopyridin-2-carboxamide and 62 mg of pyridine was introduced to 3 ml of tetrahydrofuran, 63 mg of benzoyl chloride was added, and the mixture was stirred at room temperature for 3 hours. Ethyl acetate was introduced, and the organic layer was washed with water and then with saturated aqueous sodium hydrogen carbonate solution. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure, and thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=6:4) to give 0.13 g (yield 65%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.36 (6H, s), 7.36 (2H, s), 7.53-7.57 (2H, m), 7.61-7.65 (1H, m), 7.95-8.03 (3H, m), 8.08 (1H, dd, J=1.0, 7.3 Hz), 8.52 (1H, broad-s), 8.62 (1H, dd, J=1.0, 8.3 Hz), 9.19 (1H, broad-s).

Example 12-4 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 6-(benzoylamino)-1-oxopyridin-2-carboxamide (Compound No. 2164)

A mixture of 65 mg of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 6-(benzoylamino)pyridin-2-carboxamide and 0.11 g of m-chloroperbenzoic acid was introduced to 5 ml of benzene, and the mixture was stirred at 80° C. for 4 hours. The mixture was cooled to room temperature, and the organic layer was washed with water and saturated aqueous sodium hydrogen carbonate solution sequentially and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=4:1) to give 52 mg (yield 52%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.34 (6H, s), 7.47 (2H, s), 7.62-7.65 (2H, m), 7.70-7.81 (2H, m), 8.00-8.04 (3H, m), 8.64 (1H, dd, J=1.5, 8.3 Hz), 10.90 (1H, broad-s), 12.30 (1H, broad-s).

Example 13-1 Preparation of 2,6-dibromo-4-heptafluoroisopropylaniline

To a solution prepared by adding 2.0 g of 4-heptafluoroisopropylaniline in 5 ml of N,N-dimethyl formamide, 2.73 g of N-bromosuccinimide dissolved in 10 ml of N,N-dimethyl formamide was introduced at 5° C. After the reaction solution was returned to room temperature and stirred for 2 hours, ethyl acetate and water were added thereto, and the organic layer was separated and washed once with water. The solvent was distilled off under reduced pressure, and thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=20:1) to give 2.20 g (yield 69%) of the title compound as an orange oil.

¹H-NMR (CDCl₃, ppm) δ 4.89 (2H, broad-s), 7.59 (2H, s).

Example 13-2 Preparation of N-(2,6-dibromo-4-heptafluoroisopropyl)phenyl 3-nitrobenzamide

A mixed solution of 2.20 g of 2,6-dibromo-4-heptafluoroisopropylaniline, 1.46 g of 3-nitrobenzoyl chloride and 10 ml of pyridine was stirred at 70° C. for 20 hours. After the solution was returned to room temperature, ethyl acetate and 1N hydrochloric acid were added, and the organic layer was separated and washed with a saturated aqueous sodium hydrogen carbonate solution. The solvent was distilled off under reduced pressure, and thus obtained residue was dissolved in a solvent mixture of 8 ml of tetrahydrofuran and 2 ml of methanol. Then, the solution was cooled to 5° C., 0.30 g of sodium hydroxide was added, the solution was stirred for 2 hours, and ethyl acetate and water were added to the reaction solution. The organic layer was separated, washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and thus obtained residue was washed with hexane to give 2.19 g (yield 73%) of the title compound as a pale brown solid.

¹H-NMR (DMSO-d₆, ppm) δ 7.92 (1H, t, J=7.8 Hz), 8.08 (2H, s), 8.45 (1H, d, J=7.8 Hz), 8.53 (1H, dd, J=1.5, 7.8 Hz), 8.85 (1H, d, J=1.5 Hz), 11.08 (1H, s).

Example 13-3 Preparation of N-(2,6-dibromo-4-heptafluoroisopropyl)phenyl 3-aminobenzamide

The title product was obtained as a white solid according to the conditions described in Example 1-2.

¹H-NMR (DMSO-d₆, ppm) δ 5.39 (2H, broad-s), 6.77-6.80 (1H, m), 7.13-7.20 (3H, m), 8.02 (2H, s), 10.35 (1H, s).

Example 13-4 Preparation of N-(2,6-dibromo-4-heptafluoroisopropyl)phenyl 3-(2-fluorobenzoyl)aminobenzamide (Compound No. 8)

The title compound was obtained as a white solid using 2-fluorobenzoyl chloride according to the conditions described in Example 1-3.

¹H-NMR (DMSO-d₆, ppm) δ 7.33-7.40 (2H, m), 7.55-7.63 (2H, m), 7.68-7.72 (1H, m), 7.78 (1H, d, J=7.8 Hz), 7.99 (1H, d, J=7.8 Hz), 8.05 (2H, s), 8.34 (1H, s), 10.65 (1H, s), 10.69 (1H, s).

Example 14-1 Preparation of 4-(heptafluoro-n-propylthio)aniline

To 20 ml of an acetonitrile solution of 1.25 g of 4-aminothiophenol and 1.11 g of triethylamine, 5.91 g of 1-iodoheptafluoro-n-propane was added, and the mixture was stirred at room temperature for 3 hours. The mixture was diluted with ether, washed with an aqueous solution of 1N sodium hydroxide and purified by silica gel column chromatography (eluent:hexane:ethyl acetate=4:1) to give 1.85 g (yield 63%) of the title compound.

¹H-NMR (CDCl₃, ppm) δ 3.95 (2H, s), 6.66 (2H, d, J=8.8 Hz), 7.40 (2H, d, J=8.8 Hz).

Example 14-2 Preparation of 2,6-dibromo-4-(heptafluoro-n-propylthio)aniline

To a solution prepared by adding 0.77 g of 4-(heptafluoro-n-propylthio)aniline in 15 ml of N,N-dimethyl formamide, 0.98 g of N-bromosuccinimide was introduced. After the mixture was stirred at 60° C. for 2 hours, ether and water were added, and the organic layer was separated. The organic layer was twice washed with water and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=9:1) to give 1.19 g (yield 100%) of the title compound as a red oil.

¹H-NMR (CDCl₃, ppm) δ 4.98 (2H, broad-s), 7.66 (2H, s).

Example 14-3 Preparation of N-(2,6-dibromo-4-heptafluoro-n-propylthio)phenyl 3-nitrobenzamide

To a solution prepared by adding 1.08 g of 2,6-dibromo-4-(heptafluoro-n-propylthio)aniline and 0.4 g of pyridine to 20 ml of tetrahydrofuran with stirring at room temperature, 0.55 g of 3-nitrobenzoyl chloride dissolved in 20 ml of tetrahydrofuran was gradually introduced dropwise. After the mixture was stirred at room temperature for 10 hours, ethyl acetate and water were added to the reaction solution. The organic layer was separated and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=4:1) to give 0.86 g (yield 48%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 7.73 (1H, s, J=7.8 Hz), 7.77 (1H, t, J=7.8 Hz), 7.96 (2H, s), 8.31 (1H, s), 8.47-8.50 (1H, m), 8.79 (1H, t, J=2.0 Hz).

Example 14-4 Preparation of N-{2,6-dibromo-4-(heptafluoro-n-propylthio)}phenyl 3-aminobenzamide (Compound No. I-28)

To a solution prepared by adding 0.97 g of N-{2,6-dibromo-4-(heptafluoro-n-propylthio)phenyl 3-nitrobenzamide and 0.95 g of anhydrous tin(II) chloride to 20 ml of ethanol with stirring at room temperature, 2 ml of concentrated hydrochloric acid was added, and the mixture was heated with stirring at 60° C. for 1 hour. After the mixture was returned to room temperature, the reaction solution was poured onto water, and neutralization was carried out using potassium carbonate. Ethyl acetate was added, the insolubles were filtered off, and the organic layer was separated and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled off under reduced pressure. Thus obtained residue was washed with hexane to give 0.75 g (yield 81%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 3.89 (2H, broad-s), 6.90 (1H, dt, J=2.5, 6.4 Hz), 7.28-7.30 (3H, m), 7.60 (1H, s), 7.93 (2H, s).

Example 14-5 Preparation of N-(2,6-dibromo-4-heptafluoro-n-propylthio)phenyl 3-(benzoylamino)benzamide (Compound No. 263)

To a solution prepared by adding 0.10 g of N-(2,6-dibromo-4-heptafluoro-n-propylthio)phenyl 3-aminobenzamide and 0.02 g of pyridine to 5 ml of tetrahydrofuran with stirring at room temperature, 0.03 g of benzoyl chloride dissolved in 1 ml of tetrahydrofuran was introduced. After the mixture was stirred at room temperature for 1 hour, ethyl acetate and 1N hydrochloric acid were added, and the organic layer was separated. The organic layer was washed once with saturated aqueous sodium hydrogen carbonate solution and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=3:1) to give 0.10 g (yield 67%) of the title compound as a white solid.

¹H-NMR (DMSO-d₆, ppm) δ 7.47-7.57 (4H, m), 7.78 (1H, d, J=7.8 Hz), 7.93 (2H, s), 7.99-8.01 (2H, m), 8.18 (1H, d, J=7.8 Hz), 8.33 (1H, t, J=2.0 Hz), 9.27 (1H, s), 9.65 (1H, s).

Example 14-6 Preparation of N-(2,6-dibromo-4-heptafluoro-n-propylthio)phenyl 3-[(2-chloropyridin-3-yl)carbonylamino]benzamide (Compound No. 309)

To a solution prepared by adding 0.15 g of N-(2,6-dibromo-4-heptafluoro-n-propylthio)phenyl 3-aminobenzamide and 0.03 g of pyridine to 5 ml of tetrahydrofuran, 0.05 g of 2-chloronicotinoyl chloride hydrochloride was added, and the mixture was stirred at room temperature for 4 hours. Ethyl acetate was added, the mixture was twice washed with saturated sodium hydrogen carbonate solution, and the solvent was distilled off under reduced pressure. Thus obtained solid was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=3:1) to give 0.17 g (yield 92%) of the title compound in an amorphous form.

¹H-NMR (CDCl₃, ppm) δ 7.44 (1H, dd, J=4.8, 7.8 Hz), 7.56 (1H, t, J=7.8 Hz), 7.80 (1H, d, J=7.8 Hz), 7.86 (1H, s), 7.92 (1H, d, J=7.8 Hz), 7.95 (2H, s), 8.23 (1H, dd, J=2.0, 7.8 Hz), 8.30 (1H, s), 8.41 (1H, s), 8.55 (1H, dd, J=2.0, 4.8 Hz).

Example 14-7 Preparation of N-(2,6-dibromo-4-heptafluoro-n-propylsulfinyl)phenyl 3-nitrobenzamide

To a solution prepared by adding 0.5 g of N-(2,6-dibromo-4-heptafluoro-n-propylthio)phenyl 3-nitrobenzamide to 15 ml of chloroform and stirring at room temperature, 0.5 g of m-chloroperbenzoic acid was introduced. The mixture was stirred at room temperature for 2 days, and after addition of an aqueous solution of sodium sulfite, the mixture was stirred again. Phase separation was carried out, an obtained organic layer was washed with an aqueous solution of sodium hydroxide and saturated brine, and the solvent was distilled off under reduced pressure. Thus obtained solid was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=4:1) to give 0.36 g (yield 70%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 7.76-7.82 (2H, m), 8.06 (1H, s), 8.29 (1H, s), 8.33-8.35 (1H, m), 8.49-8.53 (1H, m), 8.81 (1H, s).

Example 14-8 Preparation of N-(2,6-dibromo-4-heptafluoro-n-propylsulfinyl)phenyl 3-aminobenzamide (Compound No. I-57)

The title compound was obtained using N-(2,6-dibromo-4-heptafluoro-n-propylsulfinyl)phenyl 3-nitrobenzamide according to the conditions described in Example 1-2.

¹H-NMR (CDCl₃, ppm) δ 6.90-6.94 (1H, m), 7.28-7.33 (3H, m), 7.73 (1H, s), 8.02 (1H, s), 8.25 (1H, s).

Example 14-9 Preparation of N-(2,6-dibromo-4-heptafluoro-n-propylsulfinyl)phenyl 3-(benzoylamino)benzamide (Compound No. 335)

The title compound was obtained using N-(2,6-dibromo-4-heptafluoro-n-propylsulfinyl)phenyl 3-aminobenzamide according to the conditions described in Example 1-3.

¹H-NMR (CDCl₃, ppm) δ7.45-7.61 (4H, m), 7.77-7.79 (1H, m), 7.87-7.91 (3H, m), 8.01 (1H, s), 8.07-8.10 (1H, m), 8.15 (1H, s), 8.25 (1H, s), 8.38 (1H, s).

Example 14-10 Preparation of 2,6-dimethyl-4-(heptafluoro-n-propylthio)aniline

A mixture of 3.0 g (1.3 mmol) of 2,6-dibromo-4-heptafluoro-n-propylthioaniline, 3.0 g (21.9 mmol) of potassium carbonate, 0.75 g (0.65 mmol) of tetrakis(triphenylphosphine)palladium and 0.17 g (1.3 mmol) of trimethylboroxine was added to 20 ml of DMF, and this was stirred at 135° C. for 6 hours. The reaction solution was returned to room temperature, the insolubles were removed by celite filtration, and filtrate was concentrated under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=12:1 to 4:1) to give 1.17 g (yield SS %) of the title compound as an oil.

¹H-NMR (CDCl₃, ppm) δ 2.17 (6H, s), 3.86 (2H, broad-s), 7.22 (2H, s).

Example 15 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(methylamino)benzamide

A mixture of 20.0 g of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-aminobenzamide, 4.40 g of an aqueous solution of 37% formaldehyde, 2.0 g of 10% palladium-carbon and 200 ml of ethyl acetate was stirred under a hydrogen atmosphere at room temperature and ambient pressure. The insolubles in the reaction solution were separated by filtration, and the filtered residue was washed with ethyl acetated. The filtrate was collected, the solvent was distilled off under reduced pressure, and thus obtained residue was washed with diisopropyl ether to give 13.5 g (yield 65%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 2.35 (6H, s), 2.91 (3H, s), 6.82 (1H, d, J=7.3 Hz), 7.18-7.52 (7H, m).

Example 16-1 Preparation of 3-(benzoylamino)benzoic acid

To a solution of 1.37 g of 3-aminobenzoic acid and 0.4 g of sodium hydroxide in 50 ml of water, 1.41 g of benzoyl chloride and a solution containing 0.4 g of sodium hydroxide in 5 ml of water were simultaneously added dropwise, in an ice bath, and the mixture was stirred at room temperature for 6 hours. The reaction solution was adjusted to pH 1 by addition of 1N hydrochloric acid, and thus obtained solid was collected by filtration to give 1.92 g (yield 80%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 7.40-7.56 (5H, m), 7.78 (1H, d, J=7.8 Hz), 8.00 (2H, d, J=8.3 Hz), 8.15 (1H, d, J=7.8 Hz), 8.35 (1H, t, J=2.0 Hz), 9.89 (1H, s).

Example 16-2 Preparation of 3-(benzoylamino)benzoyl chloride

To a suspension of 1.5 g of 3-(benzoylamino)benzoic acid in 10 ml of toluene, 2 ml of thionyl chloride was added, and the mixture was stirred under reflux conditions for 2 hours. After the mixture was returned to room temperature, the solvent was distilled off under reduced pressure to give 1.53 g (yield 95%) of the title compound as a white solid.

¹H-NMR (CDCl₃, ppm) δ 7.51-7.62 (4H, m), 7.90 (2H, d, J=7.3 Hz), 7.93 (1H, s), 7.97 (1H, s), 8.15 (1H, dt, J=1.0, 5.9 Hz), 8.28 (1H, t, J=2.0 Hz).

Using readily available benzoic acids, the following compounds can be prepared according to the processes described in Examples 16-1 and 16-2:

-   3-[(2-fluorobenzoyl)amino]benzoyl chloride -   3-[(3-fluorobenzoyl)amino]benzoyl chloride -   3-[(4-fluorobenzoyl)amino]benzoyl chloride -   3-[(2-chlorobenzoyl)amino]benzoyl chloride -   3-[(3-chlorobenzoyl)amino]benzoyl chloride -   3-[(4-chlorobenzoyl)amino]benzoyl chloride -   3-[(3-cyanobenzoyl)amino]benzoyl chloride -   3-[(4-cyanobenzoyl)amino]benzoyl chloride -   3-[(2-methyl benzoyl)amino]benzoyl chloride -   3-[(3-methyl benzoyl)amino]benzoyl chloride -   3-[(4-methyl benzoyl)amino]benzoyl chloride -   3-[(2-nitro benzoyl)amino]benzoyl chloride -   3-[(3-nitrobenzoyl)amino]benzoyl chloride -   3-[(4-nitrobenzoyl)amino]benzoyl chloride -   3-[(2-trifluoromethyl benzoyl)amino]benzoyl chloride -   3-[(3-trifluoromethyl benzoyl)amino]benzoyl chloride -   3-[(4-trifluoromethyl benzoyl)amino]benzoyl chloride -   3-[(2-trifluoromethoxy benzoyl)amino]benzoyl chloride -   3-[(3-trifluoromethoxy benzoyl)amino]benzoyl chloride -   3-[(4-trifluoromethoxy benzoyl)amino]benzoyl chloride -   3-[(2,3-difluorobenzoyl)amino]benzoyl chloride -   3-[(2,4-difluorobenzoyl)amino]benzoyl chloride -   3-[(2,5-difluorobenzoyl)amino]benzoyl chloride -   3-[(2,6-difluorobenzoyl)amino]benzoyl chloride -   3-[(3,4-difluorobenzoyl)amino]benzoyl chloride -   3-[(pyridin-3-yl)carbonylamino]benzoyl chloride -   3-[(2-fluoropyridin-3-yl)carbonylamino]benzoyl chloride -   3-[(2-chloropyridin-3-yl)carbonylamino]benzoyl chloride -   3-[(2,4-dichlorobenzoyl)amino]benzoyl chloride -   3-[(2,6-dichlorobenzoyl)amino]benzoyl chloride -   3-[(3,4-dichlorobenzoyl)amino]benzoyl chloride -   3-[(2-chloro-4-fluorobenzoyl)amino]benzoyl chloride -   3-[(4-chloro-2-fluorobenzoyl)amino]benzoyl chloride -   3-[(2-chloro-6-fluorobenzoyl)amino]benzoyl chloride -   3-[(2,3,6-trifluorobenzoyl)amino]benzoyl chloride

Example 16-3 Preparation of N-(2,6-dimethyl-4-heptafluoro-n-propylthio)phenyl 3-(benzoylamino)benzamide (Compound No. 260)

To a solution prepared by adding 0.1 g of 2,6-dimethyl-4-(heptafluoro-n-propylthio)aniline and 0.03 g of pyridine to 5 ml of tetrahydrofuran and stirring at room temperature, 0.09 g of 3-(benzoylamino)benzoyl chloride dissolved in 1 ml of tetrahydrofuran was introduced. After the mixture was stirred at room temperature for 1 hour, ethyl acetate and 1N hydrochloric acid were added, and the organic layer was separated. The organic layer was washed once with a saturated aqueous sodium hydrogen carbonate solution and dried over anhydrous magnesium sulfate. This solution was filtered, the filtrate was collected, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=3:1) to give 0.10 g (yield 53%) of the title compound as a white solid.

¹H-NMR (DMSO-d₆, ppm) δ2.31 (6H, s), 7.41 (2H, s), 7.50-7.67 (5H, m), 7.71 (1H, d, J=7.8 Hz), 7.87-7.90 (3H, m), 8.07 (1H, s), 8.31 (1H, s).

Example 17-1 Preparation of 2,6-dimethyl-4-[1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]aniline

At room temperature, 24.4 g of 2,6-dimethylaniline and 50.0 g of hexafluoroacetone hydrate were mixed, and 0.5 g of p-toluenesulfonic acid monohydrate was added. The reaction solution was stirred and heated to 100° C. After the loss of the starting material was confirmed through TLC, ethyl acetate and an aqueous solution of 1N sodium hydroxide were added to the reaction solution, and phase separation was carried out. The organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure, and the residue was washed by addition of hexane. The suspension was filtered, and thus obtained filtered residue was dried under reduced pressure at room temperature to give 24.3 g (yield 69%) of the title compound as a powder form.

¹H-NMR (CDCl₃, ppm) δ 2.20 (6H, s), 3.26 (1H, broad-s), 3.76 (2H, broad-s), 7.25 (2H, s).

Example 17-2 Preparation of N-[2,6-dimethyl-4-{(1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-nitrobenzamide (Compound No. I-124)

At room temperature, 5.0 g of 2,6-dimethyl-4-[1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]aniline, 3.9 g of 3-nitrobenzoyl chloride and 2.1 g of pyridine were introduced to 50 ml of tetrahydrofuran in a reactor, and the mixture was stirred at room temperature. After the loss of the starting material was confirmed through TLC, a saturated sodium hydrogen carbonate solution was added to the reaction solution and the solution was stirred for a while. Subsequently, ethyl acetate and water were added to the reaction solution, and phase separation was carried out. The separated organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and dried, and thus obtained residue was grinded to give 7.5 g (yield 95%) of the title compound as a powder form.

¹H-NMR (DMSO-d₆, ppm) δ 2.26 (6H, s), 7.46 (2H, s), 7.88 (1H, t, J=7.8 Hz), 8.43-8.48 (2H, m), 8.73 (1H, s), 8.81 (1H, s), 10.27 (1H, s).

Example 17-3 Preparation of N-[2,6-dimethyl-4-{1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-aminobenzamide (Compound No. I-204)

A solution prepared by adding 8.0 g of N-[2,6-dimethyl-4-{1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-aminobenzamide and 0.8 g of 10% palladium-carbon to 50 ml of methanol, was stirred at room temperature under a hydrogen atmosphere. After the loss of the starting material was confirmed through TLC, the reaction solution filtered, and thus obtained filtrate was concentrated under reduced pressure. Thus obtained residue was purified by silica gel chromatography (eluent:hexane:ethyl acetate=3:1) to give 6.3 g (yield 85%) of the title compound as a powder form.

¹H-NMR (DMSO-d₆, ppm) δ 2.35 (6H, s), 4.31 (2H, broad), 6.84-6.87 (1H, m), 7.21-7.25 (1H, m), 7.29-7.31 (2H, m), 7.47-7.49 (2H, m), 7.83 (1H, s), 8.94 (1H, s).

Example 17-4 Preparation of N-[2,6-dimethyl-4-{1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-(benzoylamino)benzamide (Compound No. I-351)

At room temperature, 6.0 g of N-[2,6-dimethyl-4-{1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-aminobenzamide, 2.5 g of benzoyl chloride and 1.8 g of pyridine were introduced to 50 ml of tetrahydrofuran. After the loss of the starting material was confirmed through TLC, the reaction solution was filtered, and thus obtained filtrate was concentrated under reduce pressure. Thus obtained residue was purified by silica gel chromatography (eluent:hexane:ethyl acetate=3:1) to give 6.3 g (yield 85%) of the title compound as a powder form.

¹H-NMR (DMSO-d₆, ppm) δ 2.26 (6H, s), 7.44 (2H, s), 7.51-7.63 (4H, m), 7.74 (1H, d, J=7.8 Hz), 7.98-8.07 (3H, m), 8.35 (1H, s), 8.71 (1H, s), 9.90 (1H, s), 10.47 (1H, s).

Using 2-fluorobenzoyl chloride instead of benzoyl chloride, N-[2,6-dimethyl-4-{1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-[(2-fluorobenzoyl)amino]benzamide (Compound No. I-358) was prepared according to Example 17-4.

¹H-NMR (DMSO-d₆, ppm) δ 2.34 (6H, s), 7.21 (1H, dd, J=8.2, 11.2 Hz), 7.32 (1H, t, J=7.8 Hz), 7.49-7.56 (4H, m), 7.78 (1H, d, J=7.8 Hz), 8.04-8.08 (2H, m), 8.23 (1H, s), 8.71 (1H, s), 9.08 (1H, d, J=11.2 Hz).

Example 17-5 Preparation of N-[2,6-dimethyl-4-{1-chloro-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-(benzoylamino)benzamide (Compound No. I-419)

At room temperature, 8.0 g of N-[2,6-dimethyl-4-{1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-(benzoylamino)benzamide and 1.0 g of pyridine were introduced to 40 ml of thionyl chloride. Then, the temperature was elevated, and the mixture was stirred under reflux conditions. After the loss of the starting material was confirmed through TLC, the reaction solution was cooled and was concentrated under reduce pressure. Thus obtained residue was purified by silica gel chromatography (eluent:hexane:ethyl acetate=3:1) to give 6.2 g (yield 75%) of the title compound as a powder form.

¹H-NMR (DMSO-d₆, ppm) δ 2.34 (6H, s), 7.49-7.63 (6H, m), 7.76 (1H, d, J=7.8 Hz), 7.99-8.08 (3H, m), 8.37 (1H, s), 9.99 (1H, s), 10.48 (1H, s).

Example 17-6 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(benzoylamino)benzamide (Compound No. 10)

At room temperature, 300 mg of N-[2,6-dimethyl-4-{1-chloro-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-(benzoylamino)benzamide and 165 mg of potassium fluoride were introduced to 20 ml of N,N-dimethyl formamide. Then, the temperature was elevated to 120° C., and the mixture was stirred for 4 hours. The reaction solution was cooled to room temperature, ethyl acetate and water were added, and the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate and filtered, and the filtrate was concentrated under reduce pressure. Thus obtained residue was washed by addition of diisopropyl ether. The suspension was filtered, and thus obtained filtered residue was dried under reduced pressure at room temperature to give 250 mg (yield 85%) of the title compound as a powder form.

The characterization is described in Example 1-3.

Example 17-7 N-[2,6-dimethyl-4-{1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-(benzoylamino)benzamide (Compound No. I-351)

At room temperature, 2.0 g of 2,6-dimethyl-4-[1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl]aniline, 2.7 g of 3-(benzoylamino)benzoyl chloride and 1.2 g of pyridine were introduced to 50 ml of tetrahydrofuran, and the mixture was stirred at room temperature. After the loss of the starting material was confirmed through TLC, a saturated aqueous sodium hydrogen carbonate solution was added to the reaction solution and the solution was stirred for a while. Subsequently, ethyl acetate and water were added to the reaction solution, and phase separation was carried out. The separated organic layer was dried over anhydrous magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure and dried, and thus obtained residue was grinded to give 3.4 g (yield 95%) of the title compound as a powder form.

The characterization is described in Example 17-4.

Example 17-8 Preparation of N-(2,6-dimethyl-4-heptafluoroisopropyl)phenyl 3-(benzoylamino)benzamide (Compound No. 10)

At room temperature, 300 mg of N-[2,6-dimethyl-4-{1-hydroxy-2,2,2-trifluoro-1-(trifluoromethyl)ethyl}phenyl]3-(benzoylamino)benzamide was introduced to 20 ml of methylene chloride. Then, 480 mg of 2,2-difluoro-1,3-dimethyl-2-imidazolidinone was added dropwise, and the mixture was stirred at room temperature for 8 hours. Water was added to the reaction solution, and the organic layer was separated. The organic layer was dried over anhydrous magnesium sulfate and filtered, and thus obtained filtrate was concentrated under reduce pressure and dried. Thus obtained solid was grinded to give 180 mg (yield 60%) of the title compound as a powder form.

The characterization is described in Example 1-3.

Example 18-1 Preparation of 4-methyl-5-nitro-2-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridine

After 1.33 g of 60% sodium hydride was introduced to 15 ml of tetrahydrofuran and cooled to 5° C., 5.84 g of 1,1,1,3,3,3-hexafluoro-2-propanol was added dropwise. The mixture was stirred at 5° C. for 30 minutes, and then 3.0 g of 2-chloro-4-methyl-5-nitropyridine dissolved in 10 ml of tetrahydrofuran was added dropwise, this being stirred at room temperature for 3 hours. After being left at room temperature for 3 days, ethyl acetate and water were added thereto, and the organic layer was separated and washed with saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=10:1) to give 4.5 g (yield 80%) of the title compound as a yellow oil.

¹H-NMR (CDCl₃, ppm) δ 2.69 (3H, s), 6.54 (1H, septet, J=6.8 Hz), 6.95 (1H, s), 8.90 (1H, s).

Example 18-2 Preparation of 5-amino-4-methyl-2-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridine

The title compound was prepared using 4-methyl-5-nitro-2-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyri dine according to the conditions described in Example 1-2.

¹H-NMR (CDCl₃, ppm) δ 2.04 (3H, s), 3.49 (2H, broad-s), 6.40 (1H, septet, J=6.3 Hz), 6.69 (1H, s), 7.54 (1H, s).

Example 18-3 Preparation of 3-amino-2-chloro-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridine

1.0 g of 5-amino-4-methyl-2-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridine was introduced to 10 ml of N,N-dimethyl formamide, and 0.56 g of N-chlorosuccinimide was added at room temperature. The temperature was elevated to 60° C., and the mixture was stirred for 1 hour and poured into water. The mixture was extracted with ethyl acetate and dried over anhydrous magnesium sulfate. The solvent was distilled off under reduced pressure, and thus obtained residue was purified by silica gel column chromatography (eluent:hexane:ethyl acetate=10:1) to give 0.50 g (yield 44%) of the title compound as a brown oil.

¹H-NMR (CDCl₃, ppm) δ 2.23 (3H, s), 3.82 (2H, broad-s), 6.24 (1H, septet, J=6.3 Hz), 6.67 (1H, s).

Example 18-4 Preparation of N-[2-chloro-4-methyl-6-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridin-3-yl]3-(benzoylamino)benzamide (Compound No. 464)

The title compound was prepared using 5-amino-4-methyl-2-(2,2,2-trifluoro-1-trifluoromethylethoxy)pyridine according to the conditions described in Example 1.

¹H-NMR (CDCl₃, ppm) δ 2.38 (3H, s), 6.34 (1H, septet, J=6.3 Hz), 6.87 (1H, s), 7.50-7.63 (5H, m), 7.72 (1H, d, J=7.8 Hz), 7.88-7.90 (3H, m), 7.99 (1H, broad-s), 8.31 (1H, broad-s).

Preparation examples containing the compound represented by Formula (1) of the invention as an active ingredient are presented in the following, but the invention is not intended to be limited thereto. Additionally, in the formulations, the unit expressed in parts mean parts by weight.

Preparation Example 1

An emulsion was obtained by homogeneously mixing, with stirring, 20 parts of the compound represented by Formula (1) of the invention, 10 parts of Sol Pol 355S (Toho Chemical Industry Co., LTD, a surfactant) and 70 parts of xylene.

Preparation Example 2

A water-dispersible powder was obtained by homogeneously mixing, with stirring, 10 parts of the compound represented by Formula (1) of the invention, 2 parts of sodium alkylnaphthalenesulfonate, 1 part of sodium ligninsulfonate, 5 parts of white carbon and 82 parts of diatomite.

Preparation Example 3

A dust formulation was obtained by homogeneously mixing, with grinding, a homogeneous mixture of 0.3 part of the compound represented by Formula (1) of the invention and 0.3 part of white carbon with 99.2 parts of clay and 0.2 part of Driless A (Sankyo Co., Ltd).

Preparation Example 4

A granule was obtained by homogeneously mixing, with grinding, 2 parts of the compound represented by Formula (1) of the invention, 2 parts of white carbon, 2 parts of sodium ligninsulfonate and 94 parts of bentonite, kneading with water, and by granulating and drying.

Preparation Example 5

A flowable formulation was prepared by sufficiently stirring and mixing 20 parts of the compound represented by Formula (1) of the invention and 5 parts of a 20% aqueous solution of polyvinyl alcohol, adding 75 parts of a 0.8% aqueous solution of xanthan gum, and stirring and mixing them again.

Furthermore, in order to confirm the excellent insecticidal activity of the compound represented by Formula (1) of the invention, Experimental Examples will be presented below, which are not intended to limit the invention anyway.

Experimental Example 1 Insecticidal Testing Against Common Cutworm (Spodoptera litura)

Cabbage leaves were immersed in a liquid comprising the testing compound to a predetermined concentration for 30 seconds and air-dried. They were placed in a 7-cm polyethylene cup, and the second-stage larvae of common cutworm were left therein. The cup was placed in a constant-temperature room at 25° C., and the survival rate was investigated after 3 days. The test was carried out with two groups of 5 larvae per group. As a result, Compound No. (to be described later) 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 16, 17, 18, 19, 20, 21, 22, 23, 25, 26, 27, 28, 29, 30, 31, 32, 33, 37, 39, 42, 43, 46, 48, 56, 57, 58, 59, 60, 61, 62, 66, 68, 69, 70, 71, 73, 74, 75, 81, 82, 83, 84, 85, 86, 87, 89, 92, 96, 99, 100, 101, 105, 106, 109, 114, 117, 122, 124, 125, 126, 127, 129, 130, 132, 136, 140, 150, 160, 163, 164, 165, 166, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 187, 188, 189, 190, 191, 192, 193, 194, 195, 196, 197, 198, 199, 200, 201, 202, 204, 207, 208, 210, 212, 256, 257, 258, 259, 260, 261, 262, 263, 266, 276, 284, 288, 309, 310, 327, 328, 329, 330, 331, 332, 333, 334, 335, 338, 369, 375, 376, 377, 378, 379, 380, 383, 414, 460, 461, 462, 463, 464, 465, 466, 467, 601, 602, 603, 604, 605, 606, 607, 609, 610, 611, 612, 616, 618, 619, 624, 628, 629, 630, 631, 633, 634, 638, 639, 649, 650, 651, 652, 653, 654, 655, 656, 657, 658, 661, 665, 668, 670, 676, 679, 682, 686, 699, 708, 711, 719, 722, 791, 1001, 1016, 1043, 1089, 1091, 1097, 1100, 1125, 1126, 1206, 1207, 1208, 1209, 1210, 1211, 1212, 1213, 1214, 1216, 1217, 1218, 1219, 1220, 1229, 1235, 1236, 1237, 1238, 1245, 1246, 1247, 1255, 1256, 1257, 1258, 1259, 1260, 1261, 1262, 1263, 1264, 1265, 1266, 1267, 1274, 1293, 1294, 1463, 1464, 1465, 1478, 1479, 1480, 1481, 1482, 1483, 1484, 1485, 1486, 1487, 1607, 1617, 1645, 1697, 2001, 2004, 2034, 2035, 2036, 2037, 2082, 2085, 2093, 2116, 2117, 2164, 2168, 2201, 2202, 2203 exhibited an pesticidal rate of 70% or more at a concentration of 100 ppm.

Experimental Example 2 Insecticidal Testing Against Diamondback Moth (Plutella xylostella)

Cabbage leaves were immersed in a liquid comprising the testing compound to a predetermined concentration for 30 seconds and air-dried. They were placed in a 7-cm polyethylene cup, and the second-stage larvae of diamondback moth were left therein. The cup was placed in a constant-temperature room at 25° C., and the survival rate was investigated after 3 days. The test was carried out with two groups of 5 larvae per group. As a result, Compound No. (to be described later) 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 17, 18, 19, 20, 21, 22, 23, 25, 26, 27, 29, 30, 31, 32, 33, 37, 39, 43, 47, 56, 58, 59, 60, 61, 62, 66, 68, 69, 70, 82, 83, 84, 85, 86, 87, 89, 92, 100, 101, 105, 106, 109, 114, 118, 122, 124, 127, 130, 132, 135, 147, 150, 154, 160, 163, 164, 165, 166, 168, 169, 170, 171, 172, 173, 174, 175, 176, 177, 178, 179, 180, 181, 182, 183, 184, 185, 186, 194, 196, 197, 198, 199, 200, 201, 202, 203, 204, 206, 207, 208, 209, 210, 212, 256, 258, 259, 260, 261, 262, 263, 266, 284, 309, 310, 314, 318, 327, 328, 329, 330, 331, 332, 333, 334, 335, 338, 369, 375, 376, 377, 378, 379, 383, 414, 460, 461, 462, 463, 464, 465, 466, 467, 601, 602, 603, 604, 605, 606, 607, 609, 610, 611, 612, 616, 618, 619, 620, 624, 628, 629, 630, 631, 633, 634, 638, 639, 650, 651, 652, 653, 654, 655, 656, 657, 665, 668, 670, 676, 679, 682, 686, 699, 708, 711, 719, 722, 791, 1001, 1016, 1043, 1089, 1091, 1097, 1100, 1125, 1126, 1206, 1207, 1208, 1209, 1210, 1211, 1212, 1213, 1214, 1215, 1216, 1217, 1218, 1219, 1220, 1229, 1235, 1236, 1237, 1238, 1245, 1246, 1247, 1255, 1256, 1257, 1258, 1259, 1260, 1261, 1262, 1263, 1264, 1265, 1266, 1267, 1274, 1293, 1294, 1463, 1464, 1465, 1478, 1479, 1480, 1481, 1482, 1484, 1485, 1486, 1487, 1607, 1617, 1645, 1697, 2001, 2034, 2037, 2082, 2085, 2093, 2116, 2117, 2164, 2168, 2201, 2202, 2203 exhibited an pesticidal rate of 70% or more at a concentration of 100 ppm.

Experimental Example 3 Insecticidal Testing Against Small Brown Planthopper (Laodelphax striatellus)

An additional test was carried out with 10 small brown planthoppers by preparing an acetone solution of the testing compound diluted to a predetermined concentration, and spraying the solution on rice paddies and air drying them. The medicament was all used as received. The paddies were placed in a constant-temperature room at 25° C., and the survival rate was investigated after 6 days. The test was carried out by means of one group of 10 pests. As a result, Compound No. (to be described later) 7, 8, 17, 25, 31, 62, 101, 105, 106, 122, 130, 164, 165, 166, 169, 170, 171, 172, 173, 174, 175, 178, 179, 180, 181, 182, 183, 184, 185, 197, 199, 201, 202, 206, 207, 208, 210, 369, 601, 604, 607, 609, 610, 611, 612, 618, 619, 620, 624, 628, 630, 633, 639, 650, 651, 652, 654, 655, 657, 665, 668, 686, 1043, 1089, 1091, 1097, 1100, 1207, 1208, 1209, 1210, 1211, 1212, 1213, 1214, 1216, 1217, 1218, 1219, 1220, 1229, 1235, 1236, 1237, 1238, 1245, 1246, 1247, 1255, 1259, 1260, 1262, 1263, 1264, 1265, 1266, 1293, 1463, 1464, 1465, 1487, 1607, 1645, 1697, 2034, 2035, 2082, 2085, 2093, 2116, 2117, 2203 exhibited an pesticidal rate of 70% or more at a concentration of 1000 ppm.

Comparative Experimental Example 1

Pesticidal testing using N-(4-heptafluoroisopropyl-2-methyl)phenyl 3-(2-iodobenzoylamino)benzamide (Compound A) and N-(2,6-dimethyl-4-trifluoromethyl)phenyl 3-(benzoylamino)benzamide (Compound B)

Additional tests were carried out using said Compound A and Compound B following the procedures of Experimental Examples 1 and 2, but insecticidal activity was not observed under the same conditions. 

The invention claimed is:
 1. A compound represented by Formula (1):

wherein A₁, A₂, A₃ and A₄ each represent a carbon atom, or A₂, A₃ and A₄ each represent a carbon atom and A₁ represents a nitrogen atom or an oxidized nitrogen atom; R₁ and R₂ each represent a hydrogen atom, an optionally substituted alkyl group or an optionally substituted C1-C4 alkylcarbonyl group; G₁ and G₂ each represent an oxygen atom or a sulfur atom; X, which may be identical or different each other, represents a hydrogen atom, a halogen atom, a C1-C3 alkyl group or a trifluoromethyl group; n is an integer of 0 to 4; Q₁ represents an optionally substituted heterocyclic group wherein the heterocyclic group herein represents a pyridyl group, a pyrimidinyl group or a pyrazyl group; and Q₂ represents a phenyl group or pyridyl group having one or more substituents, at least one of the substituent being any of a C1-C4 haloalkoxy group, a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group and a C1-C6 perfluoroalkylsulfonyl group.
 2. The compound according to claim 1 represented by Formula (1), wherein R₁ and R₂ are each a hydrogen atom or a C1-C4 alkyl group; Xs, which may be identical or different each other, are a hydrogen atom, a halogen atom or a trifluoromethyl group; Q₁ is a heterocyclic group wherein the heterocyclic group herein represents a pyridyl group, a pyrimidinyl group, a pyrazyl group, or a substituted heterocyclic group, which the heterocyclic group means the same as those described above, having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group, and a phenyl group; Q₂ is represented by Formula (2):

wherein Y₁ and Y₅, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₃ represents a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group or a C1-C6 perfluoroalkylsulfonyl group; and Y₂ and Y₄ each represent a hydrogen atom, a halogen atom or a C1-C4 alkyl group; or by Formula (3):

wherein Y₆ and Y₉, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl or a cyano group; Y₈ represents a C1-C4 haloalkoxy group, a C2-C6 perfluoroalkyl group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group or a C1-C6 perfluoroalkylsulfonyl group; and Y₇ represents a hydrogen atom, a halogen atom or a C1-C4 alkyl group.
 3. The compound according to claim 2, represented by Formula (1a), which is Formula (1) with A₁, A₂, A₃ and A₄ being all carbon atoms:

wherein R₁, R₂, G₁, G₂ and Q₁ have the same meanings as those described in claim 2, and Q₂ is represented either by Formula (2):

wherein Y₁ and Y₅, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₃ represents a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group, a C1-C6 perfluoroalkylsulfonyl group or a C2-C6 perfluoroalkyl group; and Y₂ and Y₄ each represent a hydrogen atom, a halogen atom or a C1-C4 alkyl group; or by Formula (3):

wherein Y₆ and Y₉, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₅ represents a C1-C4 haloalkoxy group, a C1-C6 perfluoroalkylthio group, a C1-C6 perfluoroalkylsulfinyl group, a C1-C6 perfluoroalkylsulfonyl group or a C2-C6 perfluoroalkyl group; and Y₇ represents a hydrogen atom, a halogen atom or a C1-C4 alkyl group, wherein in Formula (1a), X₁ and X₂ each represent a hydrogen atom or a fluorine atom; and X₃ and X₄ represent a hydrogen atom.
 4. The compound according to claim 3, represented by Formula (1a), which is Formula (1) with A₁, A₂, A₃ and A₄ being all carbon atoms:

wherein Q₂ is represented either by Formula (2):

wherein Y₁ and Y₅, which may be identical or different, each represent a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group or a cyano group; Y₃ represents a C2-C6 perfluoroalkyl group; and Y₂ and Y₄ each represent a hydrogen atom, a halogen atom or a C1-C4 alkyl group; X₁ and X₂ each represent a hydrogen atom or a fluorine atom; X₃ and X₄ represent a hydrogen atom; G₁ and G₂ each represent an oxygen atom; and Q₁ represents a heterocyclic group wherein the heterocyclic group herein represents a pyridyl group, a pyrimidinyl group, a pyrazyl group, or a substituted heterocyclic group, which the heterocyclic group means the same as those described above, having one or more substituents, which may be identical or different, selected from a halogen atom, a C1-C4 alkyl group, a C1-C4 haloalkyl group, a C2-C4 alkenyl group, a C2-C4 haloalkenyl group, a C2-C4 alkynyl group, a C2-C4 haloalkynyl group, a C3-C6 cycloalkyl group, a C3-C6 halocycloalkyl group, a C1-C3 alkoxy group, a C1-C3 haloalkoxy group, a C1-C3 alkylthio group, a C1-C3 haloalkylthio group, a C1-C3 alkylsulfinyl group, a C1-C3 haloalkylsulfinyl group, a C1-C3 alkylsulfonyl group, a C1-C3 haloalkylsulfonyl group, a C1-C4 alkylamino group, a di-C1-C4-alkylamino group, a cyano group, a nitro group, a hydroxyl group, a C1-C4 alkylcarbonyl group, a C1-C4 alkylcarbonyloxy group, a C1-C4 alkoxycarbonyl group, an acetylamino group and a phenyl group.
 5. An insecticide containing the compound according to claim 1 as the active ingredient.
 6. A method of using pesticide in treating crops for cultivation or the soil to be treated with an effective amount of the compound according to claim 1, in order to protect the crops from harmful organisms. 